Canonical Allele Identifier: CA416691182
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24194552C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23868062C>T , CM000663.2:g.23868062C>T GRCh38
NC_000001.10:g.24194552C>T , CM000663.1:g.24194552C>T GRCh37
NC_000001.9:g.24067139C>T NCBI36
NG_013346.1:g.5308G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.225G>A MANE Select ENSP00000363603.3:p.Glu75=
ENST00000374479.3:c.225G>A ENSP00000363603.3:p.Glu75=
NM_000147.4:c.225G>A NP_000138.2:p.Glu75=
XM_005245821.1:c.-325G>A XP_005245878.1:n.-325G>A
XM_005245821.3:c.-325G>A XP_005245878.1:n.-325G>A
NM_000147.5:c.225G>A MANE Select NP_000138.2:p.Glu75=
NR_174379.1:n.229G>A
NR_174380.1:n.229G>A
NR_174381.1:n.229G>A
NR_174382.1:n.229G>A