Canonical Allele Identifier: CA1158990279
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865906G= , CM000663.2:g.23865906G= GRCh38
NC_000001.10:g.24192396G= , CM000663.1:g.24192396G= GRCh37
NC_000001.9:g.24064983G= NCBI36
NG_013346.1:g.7464C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.390-281C= MANE Select ENSP00000363603.3:n.390-281C=
ENST00000374479.3:c.390-281C= ENSP00000363603.3:n.390-281C=
NM_000147.4:c.390-281C= NP_000138.2:n.390-281C=
XM_005245821.1:c.15-281C= XP_005245878.1:n.15-281C=
XM_011541167.1:c.-245+4C= XP_011539469.1:n.-245+4C=
XM_005245821.3:c.15-281C= XP_005245878.1:n.15-281C=
XM_011541167.3:c.-245+4C= XP_011539469.1:n.-245+4C=
XM_017000905.2:c.87-281C= XP_016856394.1:n.87-281C=
NM_000147.5:c.390-281C= MANE Select NP_000138.2:n.390-281C=
NR_174379.1:n.568-281C=
NR_174380.1:n.617-281C=
NR_174381.1:n.455+4C=
NR_174382.1:n.852+4C=