Canonical Allele Identifier: CA1158990119
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865393A= , CM000663.2:g.23865393A= GRCh38
NC_000001.10:g.24191883A= , CM000663.1:g.24191883A= GRCh37
NC_000001.9:g.24064470A= NCBI36
NG_013346.1:g.7977T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.524+98T= MANE Select ENSP00000363603.3:n.524+98T=
ENST00000374479.3:c.524+98T= ENSP00000363603.3:n.524+98T=
NM_000147.4:c.524+98T= NP_000138.2:n.524+98T=
XM_005245821.1:c.149+98T= XP_005245878.1:n.149+98T=
XM_011541167.1:c.-110+98T= XP_011539469.1:n.-110+98T=
XM_005245821.3:c.149+98T= XP_005245878.1:n.149+98T=
XM_011541167.3:c.-110+98T= XP_011539469.1:n.-110+98T=
XM_017000905.2:c.221+98T= XP_016856394.1:n.221+98T=
NM_000147.5:c.524+98T= MANE Select NP_000138.2:n.524+98T=
NR_174379.1:n.702+98T=
NR_174380.1:n.751+98T=
NR_174381.1:n.590+98T=
NR_174382.1:n.987+98T=