Canonical Allele Identifier: CA416605279
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24191989G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865499G>T , CM000663.2:g.23865499G>T GRCh38
NC_000001.10:g.24191989G>T , CM000663.1:g.24191989G>T GRCh37
NC_000001.9:g.24064576G>T NCBI36
NG_013346.1:g.7871C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.516C>A MANE Select ENSP00000363603.3:p.Leu172=
ENST00000374479.3:c.516C>A ENSP00000363603.3:p.Leu172=
NM_000147.4:c.516C>A NP_000138.2:p.Leu172=
XM_005245821.1:c.141C>A XP_005245878.1:p.Leu47=
XM_011541167.1:c.-118C>A XP_011539469.1:n.-118C>A
XM_005245821.3:c.141C>A XP_005245878.1:p.Leu47=
XM_011541167.3:c.-118C>A XP_011539469.1:n.-118C>A
XM_017000905.2:c.213C>A XP_016856394.1:p.Leu71=
NM_000147.5:c.516C>A MANE Select NP_000138.2:p.Leu172=
NR_174379.1:n.694C>A
NR_174380.1:n.743C>A
NR_174381.1:n.582C>A
NR_174382.1:n.979C>A