Canonical Allele Identifier: CA1845638843
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648399G= , CM000671.2:g.34648399G= GRCh38
NC_000009.11:g.34648396G= , CM000671.1:g.34648396G= GRCh37
NC_000009.10:g.34638396G= NCBI36
NG_009029.1:g.6762G=
NG_028966.1:g.1215G=
NG_009029.2:g.6811G=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*218G= ENSP00000509954.1:n.*218G=
ENST00000378842.8:c.630G= MANE Select ENSP00000368119.4:p.Lys210=
ENST00000378842.7:c.630G= ENSP00000368119.3:p.Lys210=
ENST00000450095.6:c.303G= ENSP00000401956.2:p.Lys101=
ENST00000472111.5:n.886G=
ENST00000473506.6:c.*218G= ENSP00000432839.2:n.*218G=
ENST00000473529.5:n.789G=
ENST00000487381.5:n.1015G=
ENST00000489643.6:n.405G=
ENST00000554085.5:c.*374G= ENSP00000450419.1:n.*374G=
ENST00000554550.5:c.*250G= ENSP00000451435.1:n.*250G=
ENST00000554638.5:n.1102G=
ENST00000555020.5:n.786G=
ENST00000555086.5:n.634G=
ENST00000555214.5:n.451G=
ENST00000556244.1:c.617G=
ENST00000556278.1:c.375G= ENSP00000451792.1:p.Lys125=
ENST00000556494.5:n.751G=
ENST00000557706.5:n.1192G=
NM_000155.3:c.630G= NP_000146.2:p.Lys210=
NM_001258332.1:c.303G= NP_001245261.1:p.Lys101=
NM_000155.4:c.630G= MANE Select NP_000146.2:p.Lys210=
NM_001258332.2:c.303G= NP_001245261.1:p.Lys101=