Canonical Allele Identifier: CA416626863
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175279T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848789T>A , CM000663.2:g.23848789T>A GRCh38
NC_000001.10:g.24175279T>A , CM000663.1:g.24175279T>A GRCh37
NC_000001.9:g.24047866T>A NCBI36
NG_013346.1:g.24581A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374479.4:c.1020A>T MANE Select ENSP00000363603.3:p.Gly340=
ENST00000374479.3:c.1020A>T ENSP00000363603.3:p.Gly340=
NM_000147.4:c.1020A>T NP_000138.2:p.Gly340=
XM_005245821.1:c.645A>T XP_005245878.1:p.Gly215=
XM_011541167.1:c.387A>T XP_011539469.1:p.Gly129=
XM_005245821.3:c.645A>T XP_005245878.1:p.Gly215=
XM_011541167.3:c.387A>T XP_011539469.1:p.Gly129=
XM_017000905.2:c.717A>T XP_016856394.1:p.Gly239=
NM_000147.5:c.1020A>T MANE Select NP_000138.2:p.Gly340=
NR_174379.1:n.1198A>T
NR_174380.1:n.1247A>T
NR_174381.1:n.1086A>T
NR_174382.1:n.1483A>T