Canonical Allele Identifier: CA339036722
Gene: FUCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1379908534
gnomAD v2: 1-24175305-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848815C>T , CM000663.2:g.23848815C>T GRCh38
NC_000001.10:g.24175305C>T , CM000663.1:g.24175305C>T GRCh37
NC_000001.9:g.24047892C>T NCBI36
NG_013346.1:g.24555G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.994G>A MANE Select ENSP00000363603.3:p.Gly332Arg
ENST00000374479.3:c.994G>A ENSP00000363603.3:p.Gly332Arg
NM_000147.4:c.994G>A NP_000138.2:p.Gly332Arg
XM_005245821.1:c.619G>A XP_005245878.1:p.Gly207Arg
XM_011541167.1:c.361G>A XP_011539469.1:p.Gly121Arg
XM_005245821.3:c.619G>A XP_005245878.1:p.Gly207Arg
XM_011541167.3:c.361G>A XP_011539469.1:p.Gly121Arg
XM_017000905.2:c.691G>A XP_016856394.1:p.Gly231Arg
NM_000147.5:c.994G>A MANE Select NP_000138.2:p.Gly332Arg
NR_174379.1:n.1172G>A
NR_174380.1:n.1221G>A
NR_174381.1:n.1060G>A
NR_174382.1:n.1457G>A