Canonical Allele Identifier: CA1158981441
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848660T= , CM000663.2:g.23848660T= GRCh38
NC_000001.10:g.24175150T= , CM000663.1:g.24175150T= GRCh37
NC_000001.9:g.24047737T= NCBI36
NG_013346.1:g.24710A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1149A= MANE Select ENSP00000363603.3:p.Thr383=
ENST00000374479.3:c.1149A= ENSP00000363603.3:p.Thr383=
NM_000147.4:c.1149A= NP_000138.2:p.Thr383=
XM_005245821.1:c.774A= XP_005245878.1:p.Thr258=
XM_011541167.1:c.516A= XP_011539469.1:p.Thr172=
XM_005245821.3:c.774A= XP_005245878.1:p.Thr258=
XM_011541167.3:c.516A= XP_011539469.1:p.Thr172=
XM_017000905.2:c.846A= XP_016856394.1:p.Thr282=
NM_000147.5:c.1149A= MANE Select NP_000138.2:p.Thr383=
NR_174379.1:n.1327A=
NR_174380.1:n.1376A=
NR_174381.1:n.1215A=
NR_174382.1:n.1612A=