Canonical Allele Identifier: CA373278174

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34646708C>A (hg19) ; chr9:g.34646711C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646711C>A , CM000671.2:g.34646711C>A	GRCh38
NC_000009.11:g.34646708C>A , CM000671.1:g.34646708C>A	GRCh37
NC_000009.10:g.34636708C>A	NCBI36
NG_009029.1:g.5074C>A
NG_009029.2:g.5123C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.7C>A	ENSP00000509954.1:p.Arg3Ser
ENST00000378842.8:c.7C>A MANE Select	ENSP00000368119.4:p.Arg3Ser
ENST00000378842.7:c.7C>A	ENSP00000368119.3:p.Arg3Ser
ENST00000450095.6:c.-196C>A	ENSP00000401956.2:n.-196C>A
ENST00000465543.6:n.44C>A
ENST00000468099.2:n.79C>A
ENST00000472111.5:n.48C>A
ENST00000473506.6:c.7C>A	ENSP00000432839.2:p.Arg3Ser
ENST00000473529.5:n.54C>A
ENST00000487381.5:n.33C>A
ENST00000489643.6:n.37C>A
ENST00000554085.5:c.7C>A	ENSP00000450419.1:p.Arg3Ser
ENST00000554139.5:n.60C>A
ENST00000554550.5:c.7C>A	ENSP00000451435.1:p.Arg3Ser
ENST00000554638.5:n.31C>A
ENST00000554897.5:c.7C>A	ENSP00000450942.1:p.Arg3Ser
ENST00000554944.5:n.37C>A
ENST00000555020.5:n.37C>A
ENST00000555214.5:n.16C>A
ENST00000556278.1:c.7C>A	ENSP00000451792.1:p.Arg3Ser
ENST00000557541.5:n.67C>A
ENST00000605275.1:n.243C>A
NM_000155.3:c.7C>A	NP_000146.2:p.Arg3Ser
NM_001258332.1:c.-196C>A	NP_001245261.1:n.-196C>A
NM_000155.4:c.7C>A MANE Select	NP_000146.2:p.Arg3Ser
NM_001258332.2:c.-196C>A	NP_001245261.1:n.-196C>A