Canonical Allele Identifier: CA373278199
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34646717G>C , CM000671.2:g.34646717G>C GRCh38
NC_000009.11:g.34646714G>C , CM000671.1:g.34646714G>C GRCh37
NC_000009.10:g.34636714G>C NCBI36
NG_009029.1:g.5080G>C
NG_009029.2:g.5129G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.13G>C ENSP00000509954.1:p.Gly5Arg
ENST00000378842.8:c.13G>C MANE Select ENSP00000368119.4:p.Gly5Arg
ENST00000378842.7:c.13G>C ENSP00000368119.3:p.Gly5Arg
ENST00000450095.6:c.-190G>C ENSP00000401956.2:n.-190G>C
ENST00000465543.6:n.50G>C
ENST00000468099.2:n.85G>C
ENST00000472111.5:n.54G>C
ENST00000473506.6:c.13G>C ENSP00000432839.2:p.Gly5Arg
ENST00000473529.5:n.60G>C
ENST00000487381.5:n.39G>C
ENST00000489643.6:n.43G>C
ENST00000554085.5:c.13G>C ENSP00000450419.1:p.Gly5Arg
ENST00000554139.5:n.66G>C
ENST00000554550.5:c.13G>C ENSP00000451435.1:p.Gly5Arg
ENST00000554638.5:n.37G>C
ENST00000554897.5:c.13G>C ENSP00000450942.1:p.Gly5Arg
ENST00000554944.5:n.43G>C
ENST00000555020.5:n.43G>C
ENST00000555214.5:n.22G>C
ENST00000556278.1:c.13G>C ENSP00000451792.1:p.Gly5Arg
ENST00000557541.5:n.73G>C
ENST00000605275.1:n.249G>C
NM_000155.3:c.13G>C NP_000146.2:p.Gly5Arg
NM_001258332.1:c.-190G>C NP_001245261.1:n.-190G>C
NM_000155.4:c.13G>C MANE Select NP_000146.2:p.Gly5Arg
NM_001258332.2:c.-190G>C NP_001245261.1:n.-190G>C