Canonical Allele Identifier: CA259315
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs111033635
MyVariant Identifiers: chr9:g.34646768A>G (hg19) chr9:g.34646771A>G (hg38)
PubMed: PMID:11754113
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646771A>G , CM000671.2:g.34646771A>G GRCh38
NC_000009.11:g.34646768A>G , CM000671.1:g.34646768A>G GRCh37
NC_000009.10:g.34636768A>G NCBI36
NG_009029.1:g.5134A>G
NG_009029.2:g.5183A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.67A>G ENSP00000509954.1:p.Thr23Ala
ENST00000378842.8:c.67A>G MANE Select ENSP00000368119.4:p.Thr23Ala
ENST00000378842.7:c.67A>G ENSP00000368119.3:p.Thr23Ala
ENST00000450095.6:c.-136A>G ENSP00000401956.2:n.-136A>G
ENST00000465543.6:n.104A>G
ENST00000468099.2:n.139A>G
ENST00000472111.5:n.108A>G
ENST00000473506.6:c.67A>G ENSP00000432839.2:p.Thr23Ala
ENST00000473529.5:n.114A>G
ENST00000487381.5:n.93A>G
ENST00000489643.6:n.97A>G
ENST00000554085.5:c.67A>G ENSP00000450419.1:p.Thr23Ala
ENST00000554139.5:n.120A>G
ENST00000554550.5:c.67A>G ENSP00000451435.1:p.Thr23Ala
ENST00000554638.5:n.91A>G
ENST00000554897.5:c.67A>G ENSP00000450942.1:p.Thr23Ala
ENST00000554944.5:n.97A>G
ENST00000555020.5:n.97A>G
ENST00000555214.5:n.76A>G
ENST00000556278.1:c.67A>G ENSP00000451792.1:p.Thr23Ala
ENST00000557541.5:n.127A>G
ENST00000605275.1:n.303A>G
NM_000155.3:c.67A>G NP_000146.2:p.Thr23Ala
NM_001258332.1:c.-136A>G NP_001245261.1:n.-136A>G
NM_000155.4:c.67A>G MANE Select NP_000146.2:p.Thr23Ala
NM_001258332.2:c.-136A>G NP_001245261.1:n.-136A>G
Search 100 bp 5'
Search 100 bp 3'