Canonical Allele Identifier: CA1845639812
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648847G= , CM000671.2:g.34648847G= GRCh38
NC_000009.11:g.34648844G= , CM000671.1:g.34648844G= GRCh37
NC_000009.10:g.34638844G= NCBI36
NG_009029.1:g.7209G=
NG_028966.1:g.1663G=
NG_009029.2:g.7259G=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*361G= ENSP00000509954.1:n.*361G=
ENST00000378842.8:c.773G= MANE Select ENSP00000368119.4:p.Arg258=
ENST00000378842.7:c.773G= ENSP00000368119.3:p.Arg258=
ENST00000450095.6:c.446G= ENSP00000401956.2:p.Arg149=
ENST00000473506.6:c.*361G= ENSP00000432839.2:n.*361G=
ENST00000489643.6:n.853G=
ENST00000554085.5:c.*517G= ENSP00000450419.1:n.*517G=
ENST00000554550.5:c.*393G= ENSP00000451435.1:n.*393G=
ENST00000554638.5:n.1245G=
ENST00000555020.5:n.1234G=
ENST00000555086.5:n.777G=
ENST00000555754.1:n.118G=
ENST00000556244.1:c.760G=
ENST00000556278.1:c.432+391G= ENSP00000451792.1:n.432+391G=
ENST00000557706.5:n.1335G=
NM_000155.3:c.773G= NP_000146.2:p.Arg258=
NM_001258332.1:c.446G= NP_001245261.1:p.Arg149=
NM_000155.4:c.773G= MANE Select NP_000146.2:p.Arg258=
NM_001258332.2:c.446G= NP_001245261.1:p.Arg149=