Canonical Allele Identifier: CA1158990156
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865490C= , CM000663.2:g.23865490C= GRCh38
NC_000001.10:g.24191980C= , CM000663.1:g.24191980C= GRCh37
NC_000001.9:g.24064567C= NCBI36
NG_013346.1:g.7880G=

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.524+1G= MANE Select ENSP00000363603.3:n.524+1G=
ENST00000374479.3:c.524+1G= ENSP00000363603.3:n.524+1G=
NM_000147.4:c.524+1G= NP_000138.2:n.524+1G=
XM_005245821.1:c.149+1G= XP_005245878.1:n.149+1G=
XM_011541167.1:c.-110+1G= XP_011539469.1:n.-110+1G=
XM_005245821.3:c.149+1G= XP_005245878.1:n.149+1G=
XM_011541167.3:c.-110+1G= XP_011539469.1:n.-110+1G=
XM_017000905.2:c.221+1G= XP_016856394.1:n.221+1G=
NM_000147.5:c.524+1G= MANE Select NP_000138.2:n.524+1G=
NR_174379.1:n.702+1G=
NR_174380.1:n.751+1G=
NR_174381.1:n.590+1G=
NR_174382.1:n.987+1G=