Canonical Allele Identifier: CA1845636351
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647579C= , CM000671.2:g.34647579C= GRCh38
NC_000009.11:g.34647576C= , CM000671.1:g.34647576C= GRCh37
NC_000009.10:g.34637576C= NCBI36
NG_009029.1:g.5942C=
NG_028966.1:g.395C=
NG_009029.2:g.5991C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.328+12C= ENSP00000509954.1:n.328+12C=
ENST00000378842.8:c.328+12C= MANE Select ENSP00000368119.4:n.328+12C=
ENST00000378842.7:c.328+12C= ENSP00000368119.3:n.328+12C=
ENST00000450095.6:c.51-253C= ENSP00000401956.2:n.51-253C=
ENST00000465543.6:n.667+12C=
ENST00000472111.5:n.381C=
ENST00000473506.6:c.279+12C= ENSP00000432839.2:n.279+12C=
ENST00000473529.5:n.387C=
ENST00000485531.1:n.566C=
ENST00000487381.5:n.587+12C=
ENST00000489643.6:n.282+321C=
ENST00000554085.5:c.*72+12C= ENSP00000450419.1:n.*72+12C=
ENST00000554139.5:n.381+12C=
ENST00000554330.5:n.288C=
ENST00000554550.5:c.253-253C= ENSP00000451435.1:n.253-253C=
ENST00000554638.5:n.597C=
ENST00000554897.5:c.253-253C= ENSP00000450942.1:n.253-253C=
ENST00000554944.5:n.321C=
ENST00000555020.5:n.358+12C=
ENST00000555086.5:n.332+12C=
ENST00000555214.5:n.261+321C=
ENST00000556157.1:n.452+12C=
ENST00000556244.1:c.315+12C=
ENST00000556278.1:c.252+321C= ENSP00000451792.1:n.252+321C=
ENST00000556403.5:n.353C=
ENST00000556494.5:n.372C=
ENST00000557541.5:n.472+12C=
ENST00000557706.5:n.687C=
NM_000155.3:c.328+12C= NP_000146.2:n.328+12C=
NM_001258332.1:c.51-253C= NP_001245261.1:n.51-253C=
NM_000155.4:c.328+12C= MANE Select NP_000146.2:n.328+12C=
NM_001258332.2:c.51-253C= NP_001245261.1:n.51-253C=