Canonical Allele Identifier: CA2579371071
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647010T>C , CM000671.2:g.34647010T>C GRCh38
NC_000009.11:g.34647007T>C , CM000671.1:g.34647007T>C GRCh37
NC_000009.10:g.34637007T>C NCBI36
NG_009029.1:g.5373T>C
NG_009029.2:g.5422T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.83-79T>C ENSP00000509954.1:n.83-79T>C
ENST00000378842.8:c.83-79T>C MANE Select ENSP00000368119.4:n.83-79T>C
ENST00000378842.7:c.83-79T>C ENSP00000368119.3:n.83-79T>C
ENST00000450095.6:c.-120-79T>C ENSP00000401956.2:n.-120-79T>C
ENST00000465543.6:n.343T>C
ENST00000468099.2:n.155-111T>C
ENST00000472111.5:n.124-79T>C
ENST00000473506.6:c.83-79T>C ENSP00000432839.2:n.83-79T>C
ENST00000473529.5:n.130-79T>C
ENST00000485531.1:n.76-79T>C
ENST00000487381.5:n.109-79T>C
ENST00000489643.6:n.113-79T>C
ENST00000554085.5:c.83-79T>C ENSP00000450419.1:n.83-79T>C
ENST00000554139.5:n.136-79T>C
ENST00000554330.5:n.80-79T>C
ENST00000554550.5:c.83-79T>C ENSP00000451435.1:n.83-79T>C
ENST00000554638.5:n.107-79T>C
ENST00000554897.5:c.83-79T>C ENSP00000450942.1:n.83-79T>C
ENST00000554944.5:n.113-79T>C
ENST00000555020.5:n.113-79T>C
ENST00000555086.5:n.87-79T>C
ENST00000555214.5:n.92-79T>C
ENST00000556157.1:n.111T>C
ENST00000556278.1:c.83-79T>C ENSP00000451792.1:n.83-79T>C
ENST00000556403.5:n.96-79T>C
ENST00000556494.5:n.115-79T>C
ENST00000557541.5:n.276-79T>C
ENST00000557706.5:n.118T>C
ENST00000605275.1:n.542T>C
NM_000155.3:c.83-79T>C NP_000146.2:n.83-79T>C
NM_001258332.1:c.-120-79T>C NP_001245261.1:n.-120-79T>C
NM_000155.4:c.83-79T>C MANE Select NP_000146.2:n.83-79T>C
NM_001258332.2:c.-120-79T>C NP_001245261.1:n.-120-79T>C