Canonical Allele Identifier: CA464403214

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648854G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648857G>A , CM000671.2:g.34648857G>A	GRCh38
NC_000009.11:g.34648854G>A , CM000671.1:g.34648854G>A	GRCh37
NC_000009.10:g.34638854G>A	NCBI36
NG_009029.1:g.7220G>A
NG_028966.1:g.1673G>A
NG_009029.2:g.7269G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*371G>A	ENSP00000509954.1:n.*371G>A
ENST00000378842.8:c.783G>A MANE Select	ENSP00000368119.4:p.Val261=
ENST00000378842.7:c.783G>A	ENSP00000368119.3:p.Val261=
ENST00000450095.6:c.456G>A	ENSP00000401956.2:p.Val152=
ENST00000473506.6:c.*371G>A	ENSP00000432839.2:n.*371G>A
ENST00000489643.6:n.863G>A
ENST00000554085.5:c.*527G>A	ENSP00000450419.1:n.*527G>A
ENST00000554550.5:c.*403G>A	ENSP00000451435.1:n.*403G>A
ENST00000554638.5:n.1255G>A
ENST00000555020.5:n.1244G>A
ENST00000555086.5:n.787G>A
ENST00000555754.1:n.128G>A
ENST00000556244.1:c.770G>A
ENST00000556278.1:c.432+401G>A	ENSP00000451792.1:n.432+401G>A
ENST00000557706.5:n.1345G>A
NM_000155.3:c.783G>A	NP_000146.2:p.Val261=
NM_001258332.1:c.456G>A	NP_001245261.1:p.Val152=
NM_000155.4:c.783G>A MANE Select	NP_000146.2:p.Val261=
NM_001258332.2:c.456G>A	NP_001245261.1:p.Val152=