Canonical Allele Identifier: CA464595866

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34647697A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647700A>G , CM000671.2:g.34647700A>G	GRCh38
NC_000009.11:g.34647697A>G , CM000671.1:g.34647697A>G	GRCh37
NC_000009.10:g.34637697A>G	NCBI36
NG_009029.1:g.6063A>G
NG_028966.1:g.516A>G
NG_009029.2:g.6112A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.329-132A>G	ENSP00000509954.1:n.329-132A>G
ENST00000378842.8:c.372A>G MANE Select	ENSP00000368119.4:p.Gly124=
ENST00000378842.7:c.372A>G	ENSP00000368119.3:p.Gly124=
ENST00000450095.6:c.51-132A>G	ENSP00000401956.2:n.51-132A>G
ENST00000465543.6:n.711A>G
ENST00000472111.5:n.502A>G
ENST00000473506.6:c.323A>G	ENSP00000432839.2:p.Glu108Gly
ENST00000473529.5:n.508A>G
ENST00000485531.1:n.687A>G
ENST00000487381.5:n.631A>G
ENST00000489643.6:n.283-415A>G
ENST00000554085.5:c.*116A>G	ENSP00000450419.1:n.*116A>G
ENST00000554139.5:n.425A>G
ENST00000554330.5:n.409A>G
ENST00000554550.5:c.253-132A>G	ENSP00000451435.1:n.253-132A>G
ENST00000554638.5:n.718A>G
ENST00000554897.5:c.253-132A>G	ENSP00000450942.1:n.253-132A>G
ENST00000554944.5:n.442A>G
ENST00000555020.5:n.402A>G
ENST00000555086.5:n.376A>G
ENST00000555214.5:n.262-348A>G
ENST00000556157.1:n.496A>G
ENST00000556244.1:c.359A>G
ENST00000556278.1:c.253-415A>G	ENSP00000451792.1:n.253-415A>G
ENST00000556403.5:n.474A>G
ENST00000556494.5:n.493A>G
ENST00000557541.5:n.516A>G
ENST00000557706.5:n.808A>G
NM_000155.3:c.372A>G	NP_000146.2:p.Gly124=
NM_001258332.1:c.51-132A>G	NP_001245261.1:n.51-132A>G
NM_000155.4:c.372A>G MANE Select	NP_000146.2:p.Gly124=
NM_001258332.2:c.51-132A>G	NP_001245261.1:n.51-132A>G