Canonical Allele Identifier: CA464404080

Gene: GALT

Linked Data

• MyVariant Identifiers: chr9:g.34649411T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649414T>A , CM000671.2:g.34649414T>A	GRCh38
NC_000009.11:g.34649411T>A , CM000671.1:g.34649411T>A	GRCh37
NC_000009.10:g.34639411T>A	NCBI36
NG_009029.1:g.7777T>A
NG_028966.1:g.2230T>A
NG_009029.2:g.7826T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*497T>A	ENSP00000509954.1:n.*497T>A
ENST00000378842.8:c.909T>A MANE Select	ENSP00000368119.4:p.Ala303=
ENST00000378842.7:c.909T>A	ENSP00000368119.3:p.Ala303=
ENST00000450095.6:c.582T>A	ENSP00000401956.2:p.Ala194=
ENST00000488412.2:n.493T>A
ENST00000489643.6:n.1317T>A
ENST00000554550.5:c.*529T>A	ENSP00000451435.1:n.*529T>A
ENST00000554638.5:n.1381T>A
ENST00000555020.5:n.1698T>A
ENST00000555754.1:n.357T>A
ENST00000556278.1:c.432+958T>A	ENSP00000451792.1:n.432+958T>A
ENST00000557706.5:n.1484T>A
NM_000155.3:c.909T>A	NP_000146.2:p.Ala303=
NM_001258332.1:c.582T>A	NP_001245261.1:p.Ala194=
NM_000155.4:c.909T>A MANE Select	NP_000146.2:p.Ala303=
NM_001258332.2:c.582T>A	NP_001245261.1:p.Ala194=