Canonical Allele Identifier: CA1158981567
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848755G= , CM000663.2:g.23848755G= GRCh38
NC_000001.10:g.24175245G= , CM000663.1:g.24175245G= GRCh37
NC_000001.9:g.24047832G= NCBI36
NG_013346.1:g.24615C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1054C= MANE Select ENSP00000363603.3:p.Gln352=
ENST00000374479.3:c.1054C= ENSP00000363603.3:p.Gln352=
NM_000147.4:c.1054C= NP_000138.2:p.Gln352=
XM_005245821.1:c.679C= XP_005245878.1:p.Gln227=
XM_011541167.1:c.421C= XP_011539469.1:p.Gln141=
XM_005245821.3:c.679C= XP_005245878.1:p.Gln227=
XM_011541167.3:c.421C= XP_011539469.1:p.Gln141=
XM_017000905.2:c.751C= XP_016856394.1:p.Gln251=
NM_000147.5:c.1054C= MANE Select NP_000138.2:p.Gln352=
NR_174379.1:n.1232C=
NR_174380.1:n.1281C=
NR_174381.1:n.1120C=
NR_174382.1:n.1517C=