Canonical Allele Identifier: CA402998006

Gene: GAMT

Linked Data

• dbSNP Id: rs1299828784
• gnomAD v4: 19-1401308-C-A
• COSMIC: COSM4686366 ; COSM4686367
• MyVariant Identifiers: chr19:g.1401307C>A (hg19) ; chr19:g.1401308C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1401308C>A , CM000681.2:g.1401308C>A	GRCh38
NC_000019.9:g.1401307C>A , CM000681.1:g.1401307C>A	GRCh37
NC_000019.8:g.1352307C>A	NCBI36
NG_009785.1:g.5246G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252288.8:c.169G>T MANE Select	ENSP00000252288.1:p.Ala57Ser
ENST00000447102.8:c.169G>T	ENSP00000403536.2:p.Ala57Ser
ENST00000640762.1:c.112+57G>T	ENSP00000492031.1:n.112+57G>T
ENST00000252288.6:c.169G>T	ENSP00000252288.1:p.Ala57Ser
ENST00000447102.7:c.169G>T	ENSP00000403536.2:p.Ala57Ser
NM_000156.5:c.169G>T	NP_000147.1:p.Ala57Ser
NM_138924.2:c.169G>T	NP_620279.1:p.Ala57Ser
NM_000156.6:c.169G>T MANE Select	NP_000147.1:p.Ala57Ser
NM_138924.3:c.169G>T	NP_620279.1:p.Ala57Ser