Canonical Allele Identifier: CA1845636399
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647622C= , CM000671.2:g.34647622C= GRCh38
NC_000009.11:g.34647619C= , CM000671.1:g.34647619C= GRCh37
NC_000009.10:g.34637619C= NCBI36
NG_009029.1:g.5985C=
NG_028966.1:g.438C=
NG_009029.2:g.6034C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.328+55C= ENSP00000509954.1:n.328+55C=
ENST00000378842.8:c.329-35C= MANE Select ENSP00000368119.4:n.329-35C=
ENST00000378842.7:c.329-35C= ENSP00000368119.3:n.329-35C=
ENST00000450095.6:c.51-210C= ENSP00000401956.2:n.51-210C=
ENST00000465543.6:n.668-35C=
ENST00000472111.5:n.424C=
ENST00000473506.6:c.280-35C= ENSP00000432839.2:n.280-35C=
ENST00000473529.5:n.430C=
ENST00000485531.1:n.609C=
ENST00000487381.5:n.588-35C=
ENST00000489643.6:n.282+364C=
ENST00000554085.5:c.*73-35C= ENSP00000450419.1:n.*73-35C=
ENST00000554139.5:n.382-35C=
ENST00000554330.5:n.331C=
ENST00000554550.5:c.253-210C= ENSP00000451435.1:n.253-210C=
ENST00000554638.5:n.640C=
ENST00000554897.5:c.253-210C= ENSP00000450942.1:n.253-210C=
ENST00000554944.5:n.364C=
ENST00000555020.5:n.359-35C=
ENST00000555086.5:n.333-35C=
ENST00000555214.5:n.261+364C=
ENST00000556157.1:n.453-35C=
ENST00000556244.1:c.316-35C=
ENST00000556278.1:c.252+364C= ENSP00000451792.1:n.252+364C=
ENST00000556403.5:n.396C=
ENST00000556494.5:n.415C=
ENST00000557541.5:n.473-35C=
ENST00000557706.5:n.730C=
NM_000155.3:c.329-35C= NP_000146.2:n.329-35C=
NM_001258332.1:c.51-210C= NP_001245261.1:n.51-210C=
NM_000155.4:c.329-35C= MANE Select NP_000146.2:n.329-35C=
NM_001258332.2:c.51-210C= NP_001245261.1:n.51-210C=