Canonical Allele Identifier: CA2775231429
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151153_44151154insGGGGCTTGGAAAACCACATG , CM000669.2:g.44151153_44151154insGGGGCTTGGAAAACCACATG GRCh38
NC_000007.13:g.44190752_44190753insGGGGCTTGGAAAACCACATG , CM000669.1:g.44190752_44190753insGGGGCTTGGAAAACCACATG GRCh37
NC_000007.12:g.44157277_44157278insGGGGCTTGGAAAACCACATG NCBI36
NG_008847.1:g.43270_43271insCATGTGGTTTTCCAAGCCCC
NG_008847.2:g.52017_52018insCATGTGGTTTTCCAAGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-79_*362-78insCATGTGGTTTTCCAAGCCCC ENSP00000379142.4:n.*362-79_*362-78insCATGTGGTTTTCCAAGCCCC
ENST00000616242.5:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC ENSP00000482149.2:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
ENST00000682635.1:n.850-79_850-78insCATGTGGTTTTCCAAGCCCC
ENST00000345378.7:c.367-79_367-78insCATGTGGTTTTCCAAGCCCC ENSP00000223366.2:n.367-79_367-78insCATGTGGTTTTCCAAGCCCC
ENST00000403799.8:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC MANE Select ENSP00000384247.3:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
ENST00000671824.1:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC ENSP00000500264.1:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
ENST00000673284.1:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC ENSP00000499852.1:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
ENST00000345378.6:c.367-79_367-78insCATGTGGTTTTCCAAGCCCC ENSP00000223366.2:n.367-79_367-78insCATGTGGTTTTCCAAGCCCC
ENST00000395796.7:c.361-79_361-78insCATGTGGTTTTCCAAGCCCC ENSP00000379142.3:n.361-79_361-78insCATGTGGTTTTCCAAGCCCC
ENST00000403799.7:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC ENSP00000384247.3:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
ENST00000437084.1:c.364-130_364-129insCATGTGGTTTTCCAAGCCCC ENSP00000402840.1:n.364-130_364-129insCATGTGGTTTTCCAAGCCCC
ENST00000616242.4:c.361-79_361-78insCATGTGGTTTTCCAAGCCCC ENSP00000482149.1:n.361-79_361-78insCATGTGGTTTTCCAAGCCCC
NM_000162.3:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC NP_000153.1:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
NM_033507.1:c.367-79_367-78insCATGTGGTTTTCCAAGCCCC NP_277042.1:n.367-79_367-78insCATGTGGTTTTCCAAGCCCC
NM_033508.1:c.361-79_361-78insCATGTGGTTTTCCAAGCCCC NP_277043.1:n.361-79_361-78insCATGTGGTTTTCCAAGCCCC
NM_000162.4:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC NP_000153.1:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
NM_001354800.1:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC NP_001341729.1:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
NM_033507.2:c.367-79_367-78insCATGTGGTTTTCCAAGCCCC NP_277042.1:n.367-79_367-78insCATGTGGTTTTCCAAGCCCC
NM_033508.2:c.361-79_361-78insCATGTGGTTTTCCAAGCCCC NP_277043.1:n.361-79_361-78insCATGTGGTTTTCCAAGCCCC
NM_000162.5:c.364-79_364-78insCATGTGGTTTTCCAAGCCCC MANE Select NP_000153.1:n.364-79_364-78insCATGTGGTTTTCCAAGCCCC
NM_033507.3:c.367-79_367-78insCATGTGGTTTTCCAAGCCCC NP_277042.1:n.367-79_367-78insCATGTGGTTTTCCAAGCCCC
NM_033508.3:c.361-79_361-78insCATGTGGTTTTCCAAGCCCC NP_277043.1:n.361-79_361-78insCATGTGGTTTTCCAAGCCCC