Canonical Allele Identifier: CA416626769
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175171C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848681C>T , CM000663.2:g.23848681C>T GRCh38
NC_000001.10:g.24175171C>T , CM000663.1:g.24175171C>T GRCh37
NC_000001.9:g.24047758C>T NCBI36
NG_013346.1:g.24689G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.1128G>A MANE Select ENSP00000363603.3:p.Arg376=
ENST00000374479.3:c.1128G>A ENSP00000363603.3:p.Arg376=
NM_000147.4:c.1128G>A NP_000138.2:p.Arg376=
XM_005245821.1:c.753G>A XP_005245878.1:p.Arg251=
XM_011541167.1:c.495G>A XP_011539469.1:p.Arg165=
XM_005245821.3:c.753G>A XP_005245878.1:p.Arg251=
XM_011541167.3:c.495G>A XP_011539469.1:p.Arg165=
XM_017000905.2:c.825G>A XP_016856394.1:p.Arg275=
NM_000147.5:c.1128G>A MANE Select NP_000138.2:p.Arg376=
NR_174379.1:n.1306G>A
NR_174380.1:n.1355G>A
NR_174381.1:n.1194G>A
NR_174382.1:n.1591G>A