Canonical Allele Identifier: CA464402941

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34648782G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648785G>A , CM000671.2:g.34648785G>A	GRCh38
NC_000009.11:g.34648782G>A , CM000671.1:g.34648782G>A	GRCh37
NC_000009.10:g.34638782G>A	NCBI36
NG_009029.1:g.7148G>A
NG_028966.1:g.1601G>A
NG_009029.2:g.7197G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.*299G>A	ENSP00000509954.1:n.*299G>A
ENST00000378842.8:c.711G>A MANE Select	ENSP00000368119.4:p.Glu237=
ENST00000378842.7:c.711G>A	ENSP00000368119.3:p.Glu237=
ENST00000450095.6:c.384G>A	ENSP00000401956.2:p.Glu128=
ENST00000473506.6:c.*299G>A	ENSP00000432839.2:n.*299G>A
ENST00000473529.5:n.870G>A
ENST00000487381.5:n.1401G>A
ENST00000489643.6:n.791G>A
ENST00000554085.5:c.*455G>A	ENSP00000450419.1:n.*455G>A
ENST00000554550.5:c.*331G>A	ENSP00000451435.1:n.*331G>A
ENST00000554638.5:n.1183G>A
ENST00000555020.5:n.1172G>A
ENST00000555086.5:n.715G>A
ENST00000555754.1:n.56G>A
ENST00000556244.1:c.698G>A
ENST00000556278.1:c.432+329G>A	ENSP00000451792.1:n.432+329G>A
ENST00000557706.5:n.1273G>A
NM_000155.3:c.711G>A	NP_000146.2:p.Glu237=
NM_001258332.1:c.384G>A	NP_001245261.1:p.Glu128=
NM_000155.4:c.711G>A MANE Select	NP_000146.2:p.Glu237=
NM_001258332.2:c.384G>A	NP_001245261.1:p.Glu128=