Canonical Allele Identifier: CA1845638796
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648389A= , CM000671.2:g.34648389A= GRCh38
NC_000009.11:g.34648386A= , CM000671.1:g.34648386A= GRCh37
NC_000009.10:g.34638386A= NCBI36
NG_009029.1:g.6752A=
NG_028966.1:g.1205A=
NG_009029.2:g.6801A=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*208A= ENSP00000509954.1:n.*208A=
ENST00000378842.8:c.620A= MANE Select ENSP00000368119.4:p.Gln207=
ENST00000378842.7:c.620A= ENSP00000368119.3:p.Gln207=
ENST00000450095.6:c.293A= ENSP00000401956.2:p.Gln98=
ENST00000472111.5:n.876A=
ENST00000473506.6:c.*208A= ENSP00000432839.2:n.*208A=
ENST00000473529.5:n.779A=
ENST00000487381.5:n.1005A=
ENST00000489643.6:n.395A=
ENST00000554085.5:c.*364A= ENSP00000450419.1:n.*364A=
ENST00000554550.5:c.*240A= ENSP00000451435.1:n.*240A=
ENST00000554638.5:n.1092A=
ENST00000554944.5:n.969A=
ENST00000555020.5:n.776A=
ENST00000555086.5:n.624A=
ENST00000555214.5:n.441A=
ENST00000556244.1:c.607A=
ENST00000556278.1:c.365A= ENSP00000451792.1:p.Gln122=
ENST00000556494.5:n.741A=
ENST00000557706.5:n.1182A=
NM_000155.3:c.620A= NP_000146.2:p.Gln207=
NM_001258332.1:c.293A= NP_001245261.1:p.Gln98=
NM_000155.4:c.620A= MANE Select NP_000146.2:p.Gln207=
NM_001258332.2:c.293A= NP_001245261.1:p.Gln98=