Canonical Allele Identifier: CA2317700494
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401487G= , CM000681.2:g.1401487G= GRCh38
NC_000019.9:g.1401486G= , CM000681.1:g.1401486G= GRCh37
NC_000019.8:g.1352486G= NCBI36
NG_009785.1:g.5067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.-11C= MANE Select ENSP00000252288.1:n.-11C=
ENST00000447102.8:c.-11C= ENSP00000403536.2:n.-11C=
ENST00000640762.1:c.-11C= ENSP00000492031.1:n.-11C=
ENST00000252288.6:c.-11C= ENSP00000252288.1:n.-11C=
ENST00000447102.7:c.-11C= ENSP00000403536.2:n.-11C=
NM_000156.5:c.-11C= NP_000147.1:n.-11C=
NM_138924.2:c.-11C= NP_620279.1:n.-11C=
NM_000156.6:c.-11C= MANE Select NP_000147.1:n.-11C=
NM_138924.3:c.-11C= NP_620279.1:n.-11C=