Canonical Allele Identifier: CA1845639942
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648867C= , CM000671.2:g.34648867C= GRCh38
NC_000009.11:g.34648864C= , CM000671.1:g.34648864C= GRCh37
NC_000009.10:g.34638864C= NCBI36
NG_009029.1:g.7230C=
NG_028966.1:g.1683C=
NG_009029.2:g.7279C=

Transcript Alleles

HGVS Amino-acid change
ENST00000691183.1:c.*381C= ENSP00000509954.1:n.*381C=
ENST00000378842.8:c.793C= MANE Select ENSP00000368119.4:p.Pro265=
ENST00000378842.7:c.793C= ENSP00000368119.3:p.Pro265=
ENST00000450095.6:c.466C= ENSP00000401956.2:p.Pro156=
ENST00000473506.6:c.*381C= ENSP00000432839.2:n.*381C=
ENST00000489643.6:n.873C=
ENST00000554085.5:c.*537C= ENSP00000450419.1:n.*537C=
ENST00000554550.5:c.*413C= ENSP00000451435.1:n.*413C=
ENST00000554638.5:n.1265C=
ENST00000555020.5:n.1254C=
ENST00000555086.5:n.797C=
ENST00000555754.1:n.138C=
ENST00000556244.1:c.780C=
ENST00000556278.1:c.432+411C= ENSP00000451792.1:n.432+411C=
ENST00000557706.5:n.1355C=
NM_000155.3:c.793C= NP_000146.2:p.Pro265=
NM_001258332.1:c.466C= NP_001245261.1:p.Pro156=
NM_000155.4:c.793C= MANE Select NP_000146.2:p.Pro265=
NM_001258332.2:c.466C= NP_001245261.1:p.Pro156=