Canonical Allele Identifier: CA464595768

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647180C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647183C>A , CM000671.2:g.34647183C>A	GRCh38
NC_000009.11:g.34647180C>A , CM000671.1:g.34647180C>A	GRCh37
NC_000009.10:g.34637180C>A	NCBI36
NG_009029.1:g.5546C>A
NG_009029.2:g.5595C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.177C>A	ENSP00000509954.1:p.Pro59=
ENST00000378842.8:c.177C>A MANE Select	ENSP00000368119.4:p.Pro59=
ENST00000378842.7:c.177C>A	ENSP00000368119.3:p.Pro59=
ENST00000450095.6:c.-26C>A	ENSP00000401956.2:n.-26C>A
ENST00000465543.6:n.516C>A
ENST00000468099.2:n.217C>A
ENST00000472111.5:n.218C>A
ENST00000473506.6:c.177C>A	ENSP00000432839.2:p.Pro59=
ENST00000473529.5:n.224C>A
ENST00000485531.1:n.170C>A
ENST00000487381.5:n.203C>A
ENST00000489643.6:n.207C>A
ENST00000554085.5:c.177C>A	ENSP00000450419.1:p.Pro59=
ENST00000554139.5:n.230C>A
ENST00000554330.5:n.174C>A
ENST00000554550.5:c.177C>A	ENSP00000451435.1:p.Pro59=
ENST00000554638.5:n.201C>A
ENST00000554897.5:c.177C>A	ENSP00000450942.1:p.Pro59=
ENST00000554944.5:n.207C>A
ENST00000555020.5:n.207C>A
ENST00000555086.5:n.181C>A
ENST00000555214.5:n.186C>A
ENST00000556157.1:n.284C>A
ENST00000556244.1:c.61C>A
ENST00000556278.1:c.177C>A	ENSP00000451792.1:p.Pro59=
ENST00000556403.5:n.190C>A
ENST00000556494.5:n.209C>A
ENST00000557541.5:n.370C>A
ENST00000557706.5:n.291C>A
NM_000155.3:c.177C>A	NP_000146.2:p.Pro59=
NM_001258332.1:c.-26C>A	NP_001245261.1:n.-26C>A
NM_000155.4:c.177C>A MANE Select	NP_000146.2:p.Pro59=
NM_001258332.2:c.-26C>A	NP_001245261.1:n.-26C>A