Canonical Allele Identifier: CA1143993292
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848707C= , CM000663.2:g.23848707C= GRCh38
NC_000001.10:g.24175197C= , CM000663.1:g.24175197C= GRCh37
NC_000001.9:g.24047784C= NCBI36
NG_013346.1:g.24663G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1102G= MANE Select ENSP00000363603.3:p.Ala368=
ENST00000374479.3:c.1102G= ENSP00000363603.3:p.Ala368=
NM_000147.4:c.1102G= NP_000138.2:p.Ala368=
XM_005245821.1:c.727G= XP_005245878.1:p.Ala243=
XM_011541167.1:c.469G= XP_011539469.1:p.Ala157=
XM_005245821.3:c.727G= XP_005245878.1:p.Ala243=
XM_011541167.3:c.469G= XP_011539469.1:p.Ala157=
XM_017000905.2:c.799G= XP_016856394.1:p.Ala267=
NM_000147.5:c.1102G= MANE Select NP_000138.2:p.Ala368=
NR_174379.1:n.1280G=
NR_174380.1:n.1329G=
NR_174381.1:n.1168G=
NR_174382.1:n.1565G=