Canonical Allele Identifier: CA1158990268
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865877A= , CM000663.2:g.23865877A= GRCh38
NC_000001.10:g.24192367A= , CM000663.1:g.24192367A= GRCh37
NC_000001.9:g.24064954A= NCBI36
NG_013346.1:g.7493T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.390-252T= MANE Select ENSP00000363603.3:n.390-252T=
ENST00000374479.3:c.390-252T= ENSP00000363603.3:n.390-252T=
NM_000147.4:c.390-252T= NP_000138.2:n.390-252T=
XM_005245821.1:c.15-252T= XP_005245878.1:n.15-252T=
XM_011541167.1:c.-245+33T= XP_011539469.1:n.-245+33T=
XM_005245821.3:c.15-252T= XP_005245878.1:n.15-252T=
XM_011541167.3:c.-245+33T= XP_011539469.1:n.-245+33T=
XM_017000905.2:c.87-252T= XP_016856394.1:n.87-252T=
NM_000147.5:c.390-252T= MANE Select NP_000138.2:n.390-252T=
NR_174379.1:n.568-252T=
NR_174380.1:n.617-252T=
NR_174381.1:n.455+33T=
NR_174382.1:n.852+33T=