Canonical Allele Identifier: CA1845638579
Gene: GALT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34648348T= , CM000671.2:g.34648348T= GRCh38
NC_000009.11:g.34648345T= , CM000671.1:g.34648345T= GRCh37
NC_000009.10:g.34638345T= NCBI36
NG_009029.1:g.6711T=
NG_028966.1:g.1164T=
NG_009029.2:g.6760T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000691183.1:c.*167T= ENSP00000509954.1:n.*167T=
ENST00000378842.8:c.579T= MANE Select ENSP00000368119.4:p.Ser193=
ENST00000378842.7:c.579T= ENSP00000368119.3:p.Ser193=
ENST00000450095.6:c.252T= ENSP00000401956.2:p.Ser84=
ENST00000472111.5:n.835T=
ENST00000473506.6:c.*167T= ENSP00000432839.2:n.*167T=
ENST00000473529.5:n.738T=
ENST00000485531.1:n.1173T=
ENST00000487381.5:n.964T=
ENST00000489643.6:n.354T=
ENST00000554085.5:c.*323T= ENSP00000450419.1:n.*323T=
ENST00000554139.5:n.825T=
ENST00000554550.5:c.*199T= ENSP00000451435.1:n.*199T=
ENST00000554638.5:n.1051T=
ENST00000554897.5:c.*266T= ENSP00000450942.1:n.*266T=
ENST00000554944.5:n.928T=
ENST00000555020.5:n.735T=
ENST00000555086.5:n.583T=
ENST00000555214.5:n.400T=
ENST00000556244.1:c.566T=
ENST00000556278.1:c.324T= ENSP00000451792.1:p.Ser108=
ENST00000556494.5:n.700T=
ENST00000557706.5:n.1141T=
NM_000155.3:c.579T= NP_000146.2:p.Ser193=
NM_001258332.1:c.252T= NP_001245261.1:p.Ser84=
NM_000155.4:c.579T= MANE Select NP_000146.2:p.Ser193=
NM_001258332.2:c.252T= NP_001245261.1:p.Ser84=