Canonical Allele Identifier: CA416605277
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24191988G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865498G>T , CM000663.2:g.23865498G>T GRCh38
NC_000001.10:g.24191988G>T , CM000663.1:g.24191988G>T GRCh37
NC_000001.9:g.24064575G>T NCBI36
NG_013346.1:g.7872C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.517C>A MANE Select ENSP00000363603.3:p.Arg173=
ENST00000374479.3:c.517C>A ENSP00000363603.3:p.Arg173=
NM_000147.4:c.517C>A NP_000138.2:p.Arg173=
XM_005245821.1:c.142C>A XP_005245878.1:p.Arg48=
XM_011541167.1:c.-117C>A XP_011539469.1:n.-117C>A
XM_005245821.3:c.142C>A XP_005245878.1:p.Arg48=
XM_011541167.3:c.-117C>A XP_011539469.1:n.-117C>A
XM_017000905.2:c.214C>A XP_016856394.1:p.Arg72=
NM_000147.5:c.517C>A MANE Select NP_000138.2:p.Arg173=
NR_174379.1:n.695C>A
NR_174380.1:n.744C>A
NR_174381.1:n.583C>A
NR_174382.1:n.980C>A