Canonical Allele Identifier: CA464401811

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34646764A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34646767A>C , CM000671.2:g.34646767A>C	GRCh38
NC_000009.11:g.34646764A>C , CM000671.1:g.34646764A>C	GRCh37
NC_000009.10:g.34636764A>C	NCBI36
NG_009029.1:g.5130A>C
NG_009029.2:g.5179A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.63A>C	ENSP00000509954.1:p.Ala21=
ENST00000378842.8:c.63A>C MANE Select	ENSP00000368119.4:p.Ala21=
ENST00000378842.7:c.63A>C	ENSP00000368119.3:p.Ala21=
ENST00000450095.6:c.-140A>C	ENSP00000401956.2:n.-140A>C
ENST00000465543.6:n.100A>C
ENST00000468099.2:n.135A>C
ENST00000472111.5:n.104A>C
ENST00000473506.6:c.63A>C	ENSP00000432839.2:p.Ala21=
ENST00000473529.5:n.110A>C
ENST00000487381.5:n.89A>C
ENST00000489643.6:n.93A>C
ENST00000554085.5:c.63A>C	ENSP00000450419.1:p.Ala21=
ENST00000554139.5:n.116A>C
ENST00000554550.5:c.63A>C	ENSP00000451435.1:p.Ala21=
ENST00000554638.5:n.87A>C
ENST00000554897.5:c.63A>C	ENSP00000450942.1:p.Ala21=
ENST00000554944.5:n.93A>C
ENST00000555020.5:n.93A>C
ENST00000555214.5:n.72A>C
ENST00000556278.1:c.63A>C	ENSP00000451792.1:p.Ala21=
ENST00000557541.5:n.123A>C
ENST00000605275.1:n.299A>C
NM_000155.3:c.63A>C	NP_000146.2:p.Ala21=
NM_001258332.1:c.-140A>C	NP_001245261.1:n.-140A>C
NM_000155.4:c.63A>C MANE Select	NP_000146.2:p.Ala21=
NM_001258332.2:c.-140A>C	NP_001245261.1:n.-140A>C