Canonical Allele Identifier: CA2582641856

Gene: GAMT

Linked Data

• gnomAD v4: 19-1401264-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1401264C>A , CM000681.2:g.1401264C>A	GRCh38
NC_000019.9:g.1401263C>A , CM000681.1:g.1401263C>A	GRCh37
NC_000019.8:g.1352263C>A	NCBI36
NG_009785.1:g.5290G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252288.8:c.181+32G>T MANE Select	ENSP00000252288.1:n.181+32G>T
ENST00000447102.8:c.181+32G>T	ENSP00000403536.2:n.181+32G>T
ENST00000640762.1:c.112+101G>T	ENSP00000492031.1:n.112+101G>T
ENST00000252288.6:c.181+32G>T	ENSP00000252288.1:n.181+32G>T
ENST00000447102.7:c.181+32G>T	ENSP00000403536.2:n.181+32G>T
NM_000156.5:c.181+32G>T	NP_000147.1:n.181+32G>T
NM_138924.2:c.181+32G>T	NP_620279.1:n.181+32G>T
NM_000156.6:c.181+32G>T MANE Select	NP_000147.1:n.181+32G>T
NM_138924.3:c.181+32G>T	NP_620279.1:n.181+32G>T