Canonical Allele Identifier: CA504895017

Gene: GAMT

Linked Data

• MyVariant Identifiers: chr19:g.1398912C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1398913C>G , CM000681.2:g.1398913C>G	GRCh38
NC_000019.9:g.1398912C>G , CM000681.1:g.1398912C>G	GRCh37
NC_000019.8:g.1349912C>G	NCBI36
NG_009785.1:g.7641G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252288.8:c.570+3G>C MANE Select	ENSP00000252288.1:n.570+3G>C
ENST00000447102.8:c.573G>C	ENSP00000403536.2:p.Val191=
ENST00000591788.3:c.253+3G>C
ENST00000640164.1:n.403+3G>C
ENST00000640762.1:c.501+3G>C	ENSP00000492031.1:n.501+3G>C
ENST00000252288.6:c.570+3G>C	ENSP00000252288.1:n.570+3G>C
ENST00000447102.7:c.573G>C	ENSP00000403536.2:p.Val191=
ENST00000591788.2:c.255+3G>C	ENSP00000466341.2:n.255+3G>C
NM_000156.5:c.570+3G>C	NP_000147.1:n.570+3G>C
NM_138924.2:c.573G>C	NP_620279.1:p.Val191=
NM_000156.6:c.570+3G>C MANE Select	NP_000147.1:n.570+3G>C
NM_138924.3:c.573G>C	NP_620279.1:p.Val191=