Canonical Allele Identifier: CA402994088

Gene: GAMT

Linked Data

• MyVariant Identifiers: chr19:g.1398929T>C (hg19) ; chr19:g.1398930T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1398930T>C , CM000681.2:g.1398930T>C	GRCh38
NC_000019.9:g.1398929T>C , CM000681.1:g.1398929T>C	GRCh37
NC_000019.8:g.1349929T>C	NCBI36
NG_009785.1:g.7624A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.556A>G MANE Select	ENSP00000252288.1:p.Thr186Ala
ENST00000447102.8:c.556A>G	ENSP00000403536.2:p.Thr186Ala
ENST00000591788.3:c.239A>G
ENST00000640164.1:n.389A>G
ENST00000640762.1:c.487A>G	ENSP00000492031.1:p.Thr163Ala
ENST00000252288.6:c.556A>G	ENSP00000252288.1:p.Thr186Ala
ENST00000447102.7:c.556A>G	ENSP00000403536.2:p.Thr186Ala
ENST00000591788.2:c.241A>G	ENSP00000466341.2:p.Thr81Ala
NM_000156.5:c.556A>G	NP_000147.1:p.Thr186Ala
NM_138924.2:c.556A>G	NP_620279.1:p.Thr186Ala
NM_000156.6:c.556A>G MANE Select	NP_000147.1:p.Thr186Ala
NM_138924.3:c.556A>G	NP_620279.1:p.Thr186Ala