Canonical Allele Identifier: CA416626806
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175215G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848725G>A , CM000663.2:g.23848725G>A GRCh38
NC_000001.10:g.24175215G>A , CM000663.1:g.24175215G>A GRCh37
NC_000001.9:g.24047802G>A NCBI36
NG_013346.1:g.24645C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1084C>T MANE Select ENSP00000363603.3:p.Leu362=
ENST00000374479.3:c.1084C>T ENSP00000363603.3:p.Leu362=
NM_000147.4:c.1084C>T NP_000138.2:p.Leu362=
XM_005245821.1:c.709C>T XP_005245878.1:p.Leu237=
XM_011541167.1:c.451C>T XP_011539469.1:p.Leu151=
XM_005245821.3:c.709C>T XP_005245878.1:p.Leu237=
XM_011541167.3:c.451C>T XP_011539469.1:p.Leu151=
XM_017000905.2:c.781C>T XP_016856394.1:p.Leu261=
NM_000147.5:c.1084C>T MANE Select NP_000138.2:p.Leu362=
NR_174379.1:n.1262C>T
NR_174380.1:n.1311C>T
NR_174381.1:n.1150C>T
NR_174382.1:n.1547C>T