Canonical Allele Identifier: CA402995438

Gene: GAMT

Linked Data

• MyVariant Identifiers: chr19:g.1399195C>A (hg19) ; chr19:g.1399196C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1399196C>A , CM000681.2:g.1399196C>A	GRCh38
NC_000019.9:g.1399195C>A , CM000681.1:g.1399195C>A	GRCh37
NC_000019.8:g.1350195C>A	NCBI36
NG_009785.1:g.7358G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252288.8:c.392-1G>T MANE Select	ENSP00000252288.1:n.392-1G>T
ENST00000447102.8:c.392-1G>T	ENSP00000403536.2:n.392-1G>T
ENST00000591788.3:c.75-1G>T
ENST00000640164.1:n.225-1G>T
ENST00000640762.1:c.323-1G>T	ENSP00000492031.1:n.323-1G>T
ENST00000252288.6:c.392-1G>T	ENSP00000252288.1:n.392-1G>T
ENST00000447102.7:c.392-1G>T	ENSP00000403536.2:n.392-1G>T
ENST00000591788.2:c.77-1G>T	ENSP00000466341.2:n.77-1G>T
NM_000156.5:c.392-1G>T	NP_000147.1:n.392-1G>T
NM_138924.2:c.392-1G>T	NP_620279.1:n.392-1G>T
NM_000156.6:c.392-1G>T MANE Select	NP_000147.1:n.392-1G>T
NM_138924.3:c.392-1G>T	NP_620279.1:n.392-1G>T