Canonical Allele Identifier: CA1158981391
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848607G= , CM000663.2:g.23848607G= GRCh38
NC_000001.10:g.24175097G= , CM000663.1:g.24175097G= GRCh37
NC_000001.9:g.24047684G= NCBI36
NG_013346.1:g.24763C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1160+42C= MANE Select ENSP00000363603.3:n.1160+42C=
ENST00000374479.3:c.1160+42C= ENSP00000363603.3:n.1160+42C=
NM_000147.4:c.1160+42C= NP_000138.2:n.1160+42C=
XM_005245821.1:c.785+42C= XP_005245878.1:n.785+42C=
XM_011541167.1:c.527+42C= XP_011539469.1:n.527+42C=
XM_005245821.3:c.785+42C= XP_005245878.1:n.785+42C=
XM_011541167.3:c.527+42C= XP_011539469.1:n.527+42C=
XM_017000905.2:c.857+42C= XP_016856394.1:n.857+42C=
NM_000147.5:c.1160+42C= MANE Select NP_000138.2:n.1160+42C=
NR_174379.1:n.1338+42C=
NR_174380.1:n.1387+42C=
NR_174381.1:n.1226+42C=
NR_174382.1:n.1623+42C=