Canonical Allele Identifier: CA464595766

Gene: GALT

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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