Canonical Allele Identifier: CA1845638791
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648388C= , CM000671.2:g.34648388C= GRCh38
NC_000009.11:g.34648385C= , CM000671.1:g.34648385C= GRCh37
NC_000009.10:g.34638385C= NCBI36
NG_009029.1:g.6751C=
NG_028966.1:g.1204C=
NG_009029.2:g.6800C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*207C= ENSP00000509954.1:n.*207C=
ENST00000378842.8:c.619C= MANE Select ENSP00000368119.4:p.Gln207=
ENST00000378842.7:c.619C= ENSP00000368119.3:p.Gln207=
ENST00000450095.6:c.292C= ENSP00000401956.2:p.Gln98=
ENST00000472111.5:n.875C=
ENST00000473506.6:c.*207C= ENSP00000432839.2:n.*207C=
ENST00000473529.5:n.778C=
ENST00000487381.5:n.1004C=
ENST00000489643.6:n.394C=
ENST00000554085.5:c.*363C= ENSP00000450419.1:n.*363C=
ENST00000554550.5:c.*239C= ENSP00000451435.1:n.*239C=
ENST00000554638.5:n.1091C=
ENST00000554944.5:n.968C=
ENST00000555020.5:n.775C=
ENST00000555086.5:n.623C=
ENST00000555214.5:n.440C=
ENST00000556244.1:c.606C=
ENST00000556278.1:c.364C= ENSP00000451792.1:p.Gln122=
ENST00000556494.5:n.740C=
ENST00000557706.5:n.1181C=
NM_000155.3:c.619C= NP_000146.2:p.Gln207=
NM_001258332.1:c.292C= NP_001245261.1:p.Gln98=
NM_000155.4:c.619C= MANE Select NP_000146.2:p.Gln207=
NM_001258332.2:c.292C= NP_001245261.1:p.Gln98=