Canonical Allele Identifier: CA259540

Gene: GALT

Linked Data

• dbSNP Id: rs111033789
• MyVariant Identifiers: chr9:g.34649456G>A (hg19) ; chr9:g.34649459G>A (hg38)
• PubMed: PMID:8956044

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34649459G>A , CM000671.2:g.34649459G>A	GRCh38
NC_000009.11:g.34649456G>A , CM000671.1:g.34649456G>A	GRCh37
NC_000009.10:g.34639456G>A	NCBI36
NG_009029.1:g.7822G>A
NG_028966.1:g.2275G>A
NG_009029.2:g.7871G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*542G>A	ENSP00000509954.1:n.*542G>A
ENST00000378842.8:c.954G>A MANE Select	ENSP00000368119.4:p.Leu318=
ENST00000378842.7:c.954G>A	ENSP00000368119.3:p.Leu318=
ENST00000450095.6:c.627G>A	ENSP00000401956.2:p.Leu209=
ENST00000488412.2:n.538G>A
ENST00000489643.6:n.1362G>A
ENST00000554550.5:c.*574G>A	ENSP00000451435.1:n.*574G>A
ENST00000554638.5:n.1426G>A
ENST00000555020.5:n.1743G>A
ENST00000555754.1:n.402G>A
ENST00000556278.1:c.432+1003G>A	ENSP00000451792.1:n.432+1003G>A
ENST00000557706.5:n.1529G>A
NM_000155.3:c.954G>A	NP_000146.2:p.Leu318=
NM_001258332.1:c.627G>A	NP_001245261.1:p.Leu209=
NM_000155.4:c.954G>A MANE Select	NP_000146.2:p.Leu318=
NM_001258332.2:c.627G>A	NP_001245261.1:p.Leu209=