Canonical Allele Identifier: CA1845638909
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648414G= , CM000671.2:g.34648414G= GRCh38
NC_000009.11:g.34648411G= , CM000671.1:g.34648411G= GRCh37
NC_000009.10:g.34638411G= NCBI36
NG_009029.1:g.6777G=
NG_028966.1:g.1230G=
NG_009029.2:g.6826G=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*233G= ENSP00000509954.1:n.*233G=
ENST00000378842.8:c.645G= MANE Select ENSP00000368119.4:p.Glu215=
ENST00000378842.7:c.645G= ENSP00000368119.3:p.Glu215=
ENST00000450095.6:c.318G= ENSP00000401956.2:p.Glu106=
ENST00000472111.5:n.901G=
ENST00000473506.6:c.*233G= ENSP00000432839.2:n.*233G=
ENST00000473529.5:n.804G=
ENST00000487381.5:n.1030G=
ENST00000489643.6:n.420G=
ENST00000554085.5:c.*389G= ENSP00000450419.1:n.*389G=
ENST00000554550.5:c.*265G= ENSP00000451435.1:n.*265G=
ENST00000554638.5:n.1117G=
ENST00000555020.5:n.801G=
ENST00000555086.5:n.649G=
ENST00000555214.5:n.466G=
ENST00000556244.1:c.632G=
ENST00000556278.1:c.390G= ENSP00000451792.1:p.Glu130=
ENST00000556494.5:n.766G=
ENST00000557706.5:n.1207G=
NM_000155.3:c.645G= NP_000146.2:p.Glu215=
NM_001258332.1:c.318G= NP_001245261.1:p.Glu106=
NM_000155.4:c.645G= MANE Select NP_000146.2:p.Glu215=
NM_001258332.2:c.318G= NP_001245261.1:p.Glu106=