Canonical Allele Identifier: CA1845638563
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648343A= , CM000671.2:g.34648343A= GRCh38
NC_000009.11:g.34648340A= , CM000671.1:g.34648340A= GRCh37
NC_000009.10:g.34638340A= NCBI36
NG_009029.1:g.6706A=
NG_028966.1:g.1159A=
NG_009029.2:g.6755A=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*162A= ENSP00000509954.1:n.*162A=
ENST00000378842.8:c.574A= MANE Select ENSP00000368119.4:p.Ser192=
ENST00000378842.7:c.574A= ENSP00000368119.3:p.Ser192=
ENST00000450095.6:c.247A= ENSP00000401956.2:p.Ser83=
ENST00000472111.5:n.830A=
ENST00000473506.6:c.*162A= ENSP00000432839.2:n.*162A=
ENST00000473529.5:n.733A=
ENST00000485531.1:n.1168A=
ENST00000487381.5:n.959A=
ENST00000489643.6:n.349A=
ENST00000554085.5:c.*318A= ENSP00000450419.1:n.*318A=
ENST00000554139.5:n.820A=
ENST00000554550.5:c.*194A= ENSP00000451435.1:n.*194A=
ENST00000554638.5:n.1046A=
ENST00000554897.5:c.*261A= ENSP00000450942.1:n.*261A=
ENST00000554944.5:n.923A=
ENST00000555020.5:n.730A=
ENST00000555086.5:n.578A=
ENST00000555214.5:n.395A=
ENST00000556244.1:c.561A=
ENST00000556278.1:c.319A= ENSP00000451792.1:p.Ser107=
ENST00000556494.5:n.695A=
ENST00000557706.5:n.1136A=
NM_000155.3:c.574A= NP_000146.2:p.Ser192=
NM_001258332.1:c.247A= NP_001245261.1:p.Ser83=
NM_000155.4:c.574A= MANE Select NP_000146.2:p.Ser192=
NM_001258332.2:c.247A= NP_001245261.1:p.Ser83=