Canonical Allele Identifier: CA341574

Gene: GAMT

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399057C>T , CM000681.2:g.1399057C>T	GRCh38
NC_000019.9:g.1399056C>T , CM000681.1:g.1399056C>T	GRCh37
NC_000019.8:g.1350056C>T	NCBI36
NG_009785.1:g.7497G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.460-31G>A MANE Select	ENSP00000252288.1:n.460-31G>A
ENST00000447102.8:c.460-31G>A	ENSP00000403536.2:n.460-31G>A
ENST00000591788.3:c.143-31G>A
ENST00000640164.1:n.293-31G>A
ENST00000640762.1:c.391-31G>A	ENSP00000492031.1:n.391-31G>A
ENST00000252288.6:c.460-31G>A	ENSP00000252288.1:n.460-31G>A
ENST00000447102.7:c.460-31G>A	ENSP00000403536.2:n.460-31G>A
ENST00000591788.2:c.145-31G>A	ENSP00000466341.2:n.145-31G>A
NM_000156.5:c.460-31G>A	NP_000147.1:n.460-31G>A
NM_138924.2:c.460-31G>A	NP_620279.1:n.460-31G>A
NM_000156.6:c.460-31G>A MANE Select	NP_000147.1:n.460-31G>A
NM_138924.3:c.460-31G>A	NP_620279.1:n.460-31G>A