Canonical Allele Identifier: CA2123465501

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416140_23416142delinsCGT , CM000676.2:g.23416140_23416142delinsCGT GRCh38
NC_000014.8:g.23885349_23885351delinsCGT , CM000676.1:g.23885349_23885351delinsCGT GRCh37
NC_000014.7:g.22955189_22955191delinsCGT NCBI36
NG_007884.1:g.24520_24522delinsACG , LRG_384:g.24520_24522delinsACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4815_4817delinsACG (MYH7) MANE Select ENSP00000347507.3:p.Thr1605=
ENST00000355349.3:c.4815_4817delinsACG (MYH7) ENSP00000347507.3:p.Thr1605=
NM_000257.3:c.4815_4817delinsACG (MYH7) NP_000248.2:p.Thr1605=
NR_126491.1:n.401_403delinsCGT (MHRT)
XM_017021340.1:c.4815_4817delinsACG (MYH7) XP_016876829.1:p.Thr1605=
NM_000257.4:c.4815_4817delinsACG (MYH7) MANE Select NP_000248.2:p.Thr1605=