Canonical Allele Identifier: CA416626857
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175270T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848780T>C , CM000663.2:g.23848780T>C GRCh38
NC_000001.10:g.24175270T>C , CM000663.1:g.24175270T>C GRCh37
NC_000001.9:g.24047857T>C NCBI36
NG_013346.1:g.24590A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.1029A>G MANE Select ENSP00000363603.3:p.Lys343=
ENST00000374479.3:c.1029A>G ENSP00000363603.3:p.Lys343=
NM_000147.4:c.1029A>G NP_000138.2:p.Lys343=
XM_005245821.1:c.654A>G XP_005245878.1:p.Lys218=
XM_011541167.1:c.396A>G XP_011539469.1:p.Lys132=
XM_005245821.3:c.654A>G XP_005245878.1:p.Lys218=
XM_011541167.3:c.396A>G XP_011539469.1:p.Lys132=
XM_017000905.2:c.726A>G XP_016856394.1:p.Lys242=
NM_000147.5:c.1029A>G MANE Select NP_000138.2:p.Lys343=
NR_174379.1:n.1207A>G
NR_174380.1:n.1256A>G
NR_174381.1:n.1095A>G
NR_174382.1:n.1492A>G