Canonical Allele Identifier: CA416626816
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175225A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848735A>C , CM000663.2:g.23848735A>C GRCh38
NC_000001.10:g.24175225A>C , CM000663.1:g.24175225A>C GRCh37
NC_000001.9:g.24047812A>C NCBI36
NG_013346.1:g.24635T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1074T>G MANE Select ENSP00000363603.3:p.Val358=
ENST00000374479.3:c.1074T>G ENSP00000363603.3:p.Val358=
NM_000147.4:c.1074T>G NP_000138.2:p.Val358=
XM_005245821.1:c.699T>G XP_005245878.1:p.Val233=
XM_011541167.1:c.441T>G XP_011539469.1:p.Val147=
XM_005245821.3:c.699T>G XP_005245878.1:p.Val233=
XM_011541167.3:c.441T>G XP_011539469.1:p.Val147=
XM_017000905.2:c.771T>G XP_016856394.1:p.Val257=
NM_000147.5:c.1074T>G MANE Select NP_000138.2:p.Val358=
NR_174379.1:n.1252T>G
NR_174380.1:n.1301T>G
NR_174381.1:n.1140T>G
NR_174382.1:n.1537T>G