Canonical Allele Identifier: CA464402078

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648363C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648366C>T , CM000671.2:g.34648366C>T	GRCh38
NC_000009.11:g.34648363C>T , CM000671.1:g.34648363C>T	GRCh37
NC_000009.10:g.34638363C>T	NCBI36
NG_009029.1:g.6729C>T
NG_028966.1:g.1182C>T
NG_009029.2:g.6778C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*185C>T	ENSP00000509954.1:n.*185C>T
ENST00000378842.8:c.597C>T MANE Select	ENSP00000368119.4:p.Ala199=
ENST00000378842.7:c.597C>T	ENSP00000368119.3:p.Ala199=
ENST00000450095.6:c.270C>T	ENSP00000401956.2:p.Ala90=
ENST00000472111.5:n.853C>T
ENST00000473506.6:c.*185C>T	ENSP00000432839.2:n.*185C>T
ENST00000473529.5:n.756C>T
ENST00000485531.1:n.1191C>T
ENST00000487381.5:n.982C>T
ENST00000489643.6:n.372C>T
ENST00000554085.5:c.*341C>T	ENSP00000450419.1:n.*341C>T
ENST00000554139.5:n.843C>T
ENST00000554550.5:c.*217C>T	ENSP00000451435.1:n.*217C>T
ENST00000554638.5:n.1069C>T
ENST00000554897.5:c.*284C>T	ENSP00000450942.1:n.*284C>T
ENST00000554944.5:n.946C>T
ENST00000555020.5:n.753C>T
ENST00000555086.5:n.601C>T
ENST00000555214.5:n.418C>T
ENST00000556244.1:c.584C>T
ENST00000556278.1:c.342C>T	ENSP00000451792.1:p.Ala114=
ENST00000556494.5:n.718C>T
ENST00000557706.5:n.1159C>T
NM_000155.3:c.597C>T	NP_000146.2:p.Ala199=
NM_001258332.1:c.270C>T	NP_001245261.1:p.Ala90=
NM_000155.4:c.597C>T MANE Select	NP_000146.2:p.Ala199=
NM_001258332.2:c.270C>T	NP_001245261.1:p.Ala90=