Canonical Allele Identifier: CA402993902

Gene: GAMT

Linked Data

• MyVariant Identifiers: chr19:g.1398907G>T (hg19) ; chr19:g.1398908G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1398908G>T , CM000681.2:g.1398908G>T	GRCh38
NC_000019.9:g.1398907G>T , CM000681.1:g.1398907G>T	GRCh37
NC_000019.8:g.1349907G>T	NCBI36
NG_009785.1:g.7646C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252288.8:c.570+8C>A MANE Select	ENSP00000252288.1:n.570+8C>A
ENST00000447102.8:c.578C>A	ENSP00000403536.2:p.Pro193Gln
ENST00000591788.3:c.253+8C>A
ENST00000640164.1:n.403+8C>A
ENST00000640762.1:c.501+8C>A	ENSP00000492031.1:n.501+8C>A
ENST00000252288.6:c.570+8C>A	ENSP00000252288.1:n.570+8C>A
ENST00000447102.7:c.578C>A	ENSP00000403536.2:p.Pro193Gln
ENST00000591788.2:c.255+8C>A	ENSP00000466341.2:n.255+8C>A
NM_000156.5:c.570+8C>A	NP_000147.1:n.570+8C>A
NM_138924.2:c.578C>A	NP_620279.1:p.Pro193Gln
NM_000156.6:c.570+8C>A MANE Select	NP_000147.1:n.570+8C>A
NM_138924.3:c.578C>A	NP_620279.1:p.Pro193Gln