Canonical Allele Identifier: CA373278773
Gene: GALT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647225T>A , CM000671.2:g.34647225T>A GRCh38
NC_000009.11:g.34647222T>A , CM000671.1:g.34647222T>A GRCh37
NC_000009.10:g.34637222T>A NCBI36
NG_009029.1:g.5588T>A
NG_028966.1:g.41T>A
NG_009029.2:g.5637T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.219T>A ENSP00000509954.1:p.Pro73=
ENST00000378842.8:c.219T>A MANE Select ENSP00000368119.4:p.Pro73=
ENST00000378842.7:c.219T>A ENSP00000368119.3:p.Pro73=
ENST00000450095.6:c.17T>A ENSP00000401956.2:p.Leu6His
ENST00000465543.6:n.558T>A
ENST00000468099.2:n.259T>A
ENST00000472111.5:n.260T>A
ENST00000473506.6:c.219T>A ENSP00000432839.2:p.Pro73=
ENST00000473529.5:n.266T>A
ENST00000485531.1:n.212T>A
ENST00000487381.5:n.245T>A
ENST00000489643.6:n.249T>A
ENST00000554085.5:c.219T>A ENSP00000450419.1:p.Pro73=
ENST00000554139.5:n.272T>A
ENST00000554330.5:n.216T>A
ENST00000554550.5:c.219T>A ENSP00000451435.1:p.Pro73=
ENST00000554638.5:n.243T>A
ENST00000554897.5:c.219T>A ENSP00000450942.1:p.Pro73=
ENST00000554944.5:n.249T>A
ENST00000555020.5:n.249T>A
ENST00000555086.5:n.223T>A
ENST00000555214.5:n.228T>A
ENST00000556157.1:n.326T>A
ENST00000556244.1:c.103T>A
ENST00000556278.1:c.219T>A ENSP00000451792.1:p.Pro73=
ENST00000556403.5:n.232T>A
ENST00000556494.5:n.251T>A
ENST00000557541.5:n.412T>A
ENST00000557706.5:n.333T>A
NM_000155.3:c.219T>A NP_000146.2:p.Pro73=
NM_001258332.1:c.17T>A NP_001245261.1:p.Leu6His
NM_000155.4:c.219T>A MANE Select NP_000146.2:p.Pro73=
NM_001258332.2:c.17T>A NP_001245261.1:p.Leu6His