Canonical Allele Identifier: CA416605284
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24191995T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865505T>G , CM000663.2:g.23865505T>G GRCh38
NC_000001.10:g.24191995T>G , CM000663.1:g.24191995T>G GRCh37
NC_000001.9:g.24064582T>G NCBI36
NG_013346.1:g.7865A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.510A>C MANE Select ENSP00000363603.3:p.Thr170=
ENST00000374479.3:c.510A>C ENSP00000363603.3:p.Thr170=
NM_000147.4:c.510A>C NP_000138.2:p.Thr170=
XM_005245821.1:c.135A>C XP_005245878.1:p.Thr45=
XM_011541167.1:c.-124A>C XP_011539469.1:n.-124A>C
XM_005245821.3:c.135A>C XP_005245878.1:p.Thr45=
XM_011541167.3:c.-124A>C XP_011539469.1:n.-124A>C
XM_017000905.2:c.207A>C XP_016856394.1:p.Thr69=
NM_000147.5:c.510A>C MANE Select NP_000138.2:p.Thr170=
NR_174379.1:n.688A>C
NR_174380.1:n.737A>C
NR_174381.1:n.576A>C
NR_174382.1:n.973A>C