Canonical Allele Identifier: CA464596013

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647955G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647958G>C , CM000671.2:g.34647958G>C	GRCh38
NC_000009.11:g.34647955G>C , CM000671.1:g.34647955G>C	GRCh37
NC_000009.10:g.34637955G>C	NCBI36
NG_009029.1:g.6321G>C
NG_028966.1:g.774G>C
NG_009029.2:g.6370G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*92G>C	ENSP00000509954.1:n.*92G>C
ENST00000378842.8:c.504G>C MANE Select	ENSP00000368119.4:p.Val168=
ENST00000378842.7:c.504G>C	ENSP00000368119.3:p.Val168=
ENST00000450095.6:c.177G>C	ENSP00000401956.2:p.Val59=
ENST00000465543.6:n.843G>C
ENST00000472111.5:n.760G>C
ENST00000473506.6:c.*92G>C	ENSP00000432839.2:n.*92G>C
ENST00000473529.5:n.640G>C
ENST00000485531.1:n.945G>C
ENST00000487381.5:n.889G>C
ENST00000489643.6:n.283-157G>C
ENST00000554085.5:c.*248G>C	ENSP00000450419.1:n.*248G>C
ENST00000554139.5:n.683G>C
ENST00000554550.5:c.*124G>C	ENSP00000451435.1:n.*124G>C
ENST00000554638.5:n.976G>C
ENST00000554897.5:c.*124G>C	ENSP00000450942.1:n.*124G>C
ENST00000554944.5:n.700G>C
ENST00000555020.5:n.660G>C
ENST00000555086.5:n.508G>C
ENST00000555214.5:n.262-90G>C
ENST00000556244.1:c.491G>C
ENST00000556278.1:c.253-157G>C	ENSP00000451792.1:n.253-157G>C
ENST00000556494.5:n.625G>C
ENST00000557706.5:n.1066G>C
NM_000155.3:c.504G>C	NP_000146.2:p.Val168=
NM_001258332.1:c.177G>C	NP_001245261.1:p.Val59=
NM_000155.4:c.504G>C MANE Select	NP_000146.2:p.Val168=
NM_001258332.2:c.177G>C	NP_001245261.1:p.Val59=