Canonical Allele Identifier: CA1158981485
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848698C= , CM000663.2:g.23848698C= GRCh38
NC_000001.10:g.24175188C= , CM000663.1:g.24175188C= GRCh37
NC_000001.9:g.24047775C= NCBI36
NG_013346.1:g.24672G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1111G= MANE Select ENSP00000363603.3:p.Ala371=
ENST00000374479.3:c.1111G= ENSP00000363603.3:p.Ala371=
NM_000147.4:c.1111G= NP_000138.2:p.Ala371=
XM_005245821.1:c.736G= XP_005245878.1:p.Ala246=
XM_011541167.1:c.478G= XP_011539469.1:p.Ala160=
XM_005245821.3:c.736G= XP_005245878.1:p.Ala246=
XM_011541167.3:c.478G= XP_011539469.1:p.Ala160=
XM_017000905.2:c.808G= XP_016856394.1:p.Ala270=
NM_000147.5:c.1111G= MANE Select NP_000138.2:p.Ala371=
NR_174379.1:n.1289G=
NR_174380.1:n.1338G=
NR_174381.1:n.1177G=
NR_174382.1:n.1574G=