Canonical Allele Identifier: CA2741604038
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401165_1401166insAA , CM000681.2:g.1401165_1401166insAA GRCh38
NC_000019.9:g.1401164_1401165insAA , CM000681.1:g.1401164_1401165insAA GRCh37
NC_000019.8:g.1352164_1352165insAA NCBI36
NG_009785.1:g.5388_5389insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.181+130_181+131insTT MANE Select ENSP00000252288.1:n.181+130_181+131insTT
ENST00000447102.8:c.181+130_181+131insTT ENSP00000403536.2:n.181+130_181+131insTT
ENST00000640762.1:c.112+199_112+200insTT ENSP00000492031.1:n.112+199_112+200insTT
ENST00000252288.6:c.181+130_181+131insTT ENSP00000252288.1:n.181+130_181+131insTT
ENST00000447102.7:c.181+130_181+131insTT ENSP00000403536.2:n.181+130_181+131insTT
NM_000156.5:c.181+130_181+131insTT NP_000147.1:n.181+130_181+131insTT
NM_138924.2:c.181+130_181+131insTT NP_620279.1:n.181+130_181+131insTT
NM_000156.6:c.181+130_181+131insTT MANE Select NP_000147.1:n.181+130_181+131insTT
NM_138924.3:c.181+130_181+131insTT NP_620279.1:n.181+130_181+131insTT