Canonical Allele Identifier: CA373278451
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647089A>C , CM000671.2:g.34647089A>C GRCh38
NC_000009.11:g.34647086A>C , CM000671.1:g.34647086A>C GRCh37
NC_000009.10:g.34637086A>C NCBI36
NG_009029.1:g.5452A>C
NG_009029.2:g.5501A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.83A>C ENSP00000509954.1:p.Asp28Ala
ENST00000378842.8:c.83A>C MANE Select ENSP00000368119.4:p.Asp28Ala
ENST00000378842.7:c.83A>C ENSP00000368119.3:p.Asp28Ala
ENST00000450095.6:c.-120A>C ENSP00000401956.2:n.-120A>C
ENST00000465543.6:n.422A>C
ENST00000468099.2:n.155-32A>C
ENST00000472111.5:n.124A>C
ENST00000473506.6:c.83A>C ENSP00000432839.2:p.Asp28Ala
ENST00000473529.5:n.130A>C
ENST00000485531.1:n.76A>C
ENST00000487381.5:n.109A>C
ENST00000489643.6:n.113A>C
ENST00000554085.5:c.83A>C ENSP00000450419.1:p.Asp28Ala
ENST00000554139.5:n.136A>C
ENST00000554330.5:n.80A>C
ENST00000554550.5:c.83A>C ENSP00000451435.1:p.Asp28Ala
ENST00000554638.5:n.107A>C
ENST00000554897.5:c.83A>C ENSP00000450942.1:p.Asp28Ala
ENST00000554944.5:n.113A>C
ENST00000555020.5:n.113A>C
ENST00000555086.5:n.87A>C
ENST00000555214.5:n.92A>C
ENST00000556157.1:n.190A>C
ENST00000556278.1:c.83A>C ENSP00000451792.1:p.Asp28Ala
ENST00000556403.5:n.96A>C
ENST00000556494.5:n.115A>C
ENST00000557541.5:n.276A>C
ENST00000557706.5:n.197A>C
ENST00000605275.1:n.621A>C
NM_000155.3:c.83A>C NP_000146.2:p.Asp28Ala
NM_001258332.1:c.-120A>C NP_001245261.1:n.-120A>C
NM_000155.4:c.83A>C MANE Select NP_000146.2:p.Asp28Ala
NM_001258332.2:c.-120A>C NP_001245261.1:n.-120A>C