Canonical Allele Identifier: CA416626792
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175201C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848711C>G , CM000663.2:g.23848711C>G GRCh38
NC_000001.10:g.24175201C>G , CM000663.1:g.24175201C>G GRCh37
NC_000001.9:g.24047788C>G NCBI36
NG_013346.1:g.24659G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1098G>C MANE Select ENSP00000363603.3:p.Gly366=
ENST00000374479.3:c.1098G>C ENSP00000363603.3:p.Gly366=
NM_000147.4:c.1098G>C NP_000138.2:p.Gly366=
XM_005245821.1:c.723G>C XP_005245878.1:p.Gly241=
XM_011541167.1:c.465G>C XP_011539469.1:p.Gly155=
XM_005245821.3:c.723G>C XP_005245878.1:p.Gly241=
XM_011541167.3:c.465G>C XP_011539469.1:p.Gly155=
XM_017000905.2:c.795G>C XP_016856394.1:p.Gly265=
NM_000147.5:c.1098G>C MANE Select NP_000138.2:p.Gly366=
NR_174379.1:n.1276G>C
NR_174380.1:n.1325G>C
NR_174381.1:n.1164G>C
NR_174382.1:n.1561G>C