Canonical Allele Identifier: CA416626753
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175150T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848660T>C , CM000663.2:g.23848660T>C GRCh38
NC_000001.10:g.24175150T>C , CM000663.1:g.24175150T>C GRCh37
NC_000001.9:g.24047737T>C NCBI36
NG_013346.1:g.24710A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1149A>G MANE Select ENSP00000363603.3:p.Thr383=
ENST00000374479.3:c.1149A>G ENSP00000363603.3:p.Thr383=
NM_000147.4:c.1149A>G NP_000138.2:p.Thr383=
XM_005245821.1:c.774A>G XP_005245878.1:p.Thr258=
XM_011541167.1:c.516A>G XP_011539469.1:p.Thr172=
XM_005245821.3:c.774A>G XP_005245878.1:p.Thr258=
XM_011541167.3:c.516A>G XP_011539469.1:p.Thr172=
XM_017000905.2:c.846A>G XP_016856394.1:p.Thr282=
NM_000147.5:c.1149A>G MANE Select NP_000138.2:p.Thr383=
NR_174379.1:n.1327A>G
NR_174380.1:n.1376A>G
NR_174381.1:n.1215A>G
NR_174382.1:n.1612A>G