Canonical Allele Identifier: CA1845635324
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34647113C= , CM000671.2:g.34647113C= GRCh38
NC_000009.11:g.34647110C= , CM000671.1:g.34647110C= GRCh37
NC_000009.10:g.34637110C= NCBI36
NG_009029.1:g.5476C=
NG_009029.2:g.5525C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.107C= ENSP00000509954.1:p.Pro36=
ENST00000378842.8:c.107C= MANE Select ENSP00000368119.4:p.Pro36=
ENST00000378842.7:c.107C= ENSP00000368119.3:p.Pro36=
ENST00000450095.6:c.-96C= ENSP00000401956.2:n.-96C=
ENST00000465543.6:n.446C=
ENST00000468099.2:n.155-8C=
ENST00000472111.5:n.148C=
ENST00000473506.6:c.107C= ENSP00000432839.2:p.Pro36=
ENST00000473529.5:n.154C=
ENST00000485531.1:n.100C=
ENST00000487381.5:n.133C=
ENST00000489643.6:n.137C=
ENST00000554085.5:c.107C= ENSP00000450419.1:p.Pro36=
ENST00000554139.5:n.160C=
ENST00000554330.5:n.104C=
ENST00000554550.5:c.107C= ENSP00000451435.1:p.Pro36=
ENST00000554638.5:n.131C=
ENST00000554897.5:c.107C= ENSP00000450942.1:p.Pro36=
ENST00000554944.5:n.137C=
ENST00000555020.5:n.137C=
ENST00000555086.5:n.111C=
ENST00000555214.5:n.116C=
ENST00000556157.1:n.214C=
ENST00000556278.1:c.107C= ENSP00000451792.1:p.Pro36=
ENST00000556403.5:n.120C=
ENST00000556494.5:n.139C=
ENST00000557541.5:n.300C=
ENST00000557706.5:n.221C=
ENST00000605275.1:n.645C=
NM_000155.3:c.107C= NP_000146.2:p.Pro36=
NM_001258332.1:c.-96C= NP_001245261.1:n.-96C=
NM_000155.4:c.107C= MANE Select NP_000146.2:p.Pro36=
NM_001258332.2:c.-96C= NP_001245261.1:n.-96C=