Canonical Allele Identifier: CA1845638559
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648341C= , CM000671.2:g.34648341C= GRCh38
NC_000009.11:g.34648338C= , CM000671.1:g.34648338C= GRCh37
NC_000009.10:g.34638338C= NCBI36
NG_009029.1:g.6704C=
NG_028966.1:g.1157C=
NG_009029.2:g.6753C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*160C= ENSP00000509954.1:n.*160C=
ENST00000378842.8:c.572C= MANE Select ENSP00000368119.4:p.Ala191=
ENST00000378842.7:c.572C= ENSP00000368119.3:p.Ala191=
ENST00000450095.6:c.245C= ENSP00000401956.2:p.Ala82=
ENST00000472111.5:n.828C=
ENST00000473506.6:c.*160C= ENSP00000432839.2:n.*160C=
ENST00000473529.5:n.731C=
ENST00000485531.1:n.1166C=
ENST00000487381.5:n.957C=
ENST00000489643.6:n.347C=
ENST00000554085.5:c.*316C= ENSP00000450419.1:n.*316C=
ENST00000554139.5:n.818C=
ENST00000554550.5:c.*192C= ENSP00000451435.1:n.*192C=
ENST00000554638.5:n.1044C=
ENST00000554897.5:c.*259C= ENSP00000450942.1:n.*259C=
ENST00000554944.5:n.921C=
ENST00000555020.5:n.728C=
ENST00000555086.5:n.576C=
ENST00000555214.5:n.393C=
ENST00000556244.1:c.559C=
ENST00000556278.1:c.317C= ENSP00000451792.1:p.Ala106=
ENST00000556494.5:n.693C=
ENST00000557706.5:n.1134C=
NM_000155.3:c.572C= NP_000146.2:p.Ala191=
NM_001258332.1:c.245C= NP_001245261.1:p.Ala82=
NM_000155.4:c.572C= MANE Select NP_000146.2:p.Ala191=
NM_001258332.2:c.245C= NP_001245261.1:p.Ala82=