Canonical Allele Identifier: CA1158981466
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848686A= , CM000663.2:g.23848686A= GRCh38
NC_000001.10:g.24175176A= , CM000663.1:g.24175176A= GRCh37
NC_000001.9:g.24047763A= NCBI36
NG_013346.1:g.24684T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.1123T= MANE Select ENSP00000363603.3:p.Trp375=
ENST00000374479.3:c.1123T= ENSP00000363603.3:p.Trp375=
NM_000147.4:c.1123T= NP_000138.2:p.Trp375=
XM_005245821.1:c.748T= XP_005245878.1:p.Trp250=
XM_011541167.1:c.490T= XP_011539469.1:p.Trp164=
XM_005245821.3:c.748T= XP_005245878.1:p.Trp250=
XM_011541167.3:c.490T= XP_011539469.1:p.Trp164=
XM_017000905.2:c.820T= XP_016856394.1:p.Trp274=
NM_000147.5:c.1123T= MANE Select NP_000138.2:p.Trp375=
NR_174379.1:n.1301T=
NR_174380.1:n.1350T=
NR_174381.1:n.1189T=
NR_174382.1:n.1586T=