Canonical Allele Identifier: CA1845636802
Gene: GALT HGNC NCBI

Linked Data

dbSNP Id: rs1821143503

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647770G>A , CM000671.2:g.34647770G>A GRCh38
NC_000009.11:g.34647767G>A , CM000671.1:g.34647767G>A GRCh37
NC_000009.10:g.34637767G>A NCBI36
NG_009029.1:g.6133G>A
NG_028966.1:g.586G>A
NG_009029.2:g.6182G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.329-62G>A ENSP00000509954.1:n.329-62G>A
ENST00000378842.8:c.378-62G>A MANE Select ENSP00000368119.4:n.378-62G>A
ENST00000378842.7:c.378-62G>A ENSP00000368119.3:n.378-62G>A
ENST00000450095.6:c.51-62G>A ENSP00000401956.2:n.51-62G>A
ENST00000465543.6:n.717-62G>A
ENST00000472111.5:n.572G>A
ENST00000473506.6:c.329-62G>A ENSP00000432839.2:n.329-62G>A
ENST00000473529.5:n.514-62G>A
ENST00000485531.1:n.757G>A
ENST00000487381.5:n.701G>A
ENST00000489643.6:n.283-345G>A
ENST00000554085.5:c.*122-62G>A ENSP00000450419.1:n.*122-62G>A
ENST00000554139.5:n.495G>A
ENST00000554330.5:n.479G>A
ENST00000554550.5:c.253-62G>A ENSP00000451435.1:n.253-62G>A
ENST00000554638.5:n.788G>A
ENST00000554897.5:c.253-62G>A ENSP00000450942.1:n.253-62G>A
ENST00000554944.5:n.512G>A
ENST00000555020.5:n.472G>A
ENST00000555086.5:n.382-62G>A
ENST00000555214.5:n.262-278G>A
ENST00000556244.1:c.365-62G>A
ENST00000556278.1:c.253-345G>A ENSP00000451792.1:n.253-345G>A
ENST00000556403.5:n.544G>A
ENST00000556494.5:n.499-62G>A
ENST00000557541.5:n.522-62G>A
ENST00000557706.5:n.878G>A
NM_000155.3:c.378-62G>A NP_000146.2:n.378-62G>A
NM_001258332.1:c.51-62G>A NP_001245261.1:n.51-62G>A
NM_000155.4:c.378-62G>A MANE Select NP_000146.2:n.378-62G>A
NM_001258332.2:c.51-62G>A NP_001245261.1:n.51-62G>A