Canonical Allele Identifier: CA416626810
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175219T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848729T>C , CM000663.2:g.23848729T>C GRCh38
NC_000001.10:g.24175219T>C , CM000663.1:g.24175219T>C GRCh37
NC_000001.9:g.24047806T>C NCBI36
NG_013346.1:g.24641A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1080A>G MANE Select ENSP00000363603.3:p.Lys360=
ENST00000374479.3:c.1080A>G ENSP00000363603.3:p.Lys360=
NM_000147.4:c.1080A>G NP_000138.2:p.Lys360=
XM_005245821.1:c.705A>G XP_005245878.1:p.Lys235=
XM_011541167.1:c.447A>G XP_011539469.1:p.Lys149=
XM_005245821.3:c.705A>G XP_005245878.1:p.Lys235=
XM_011541167.3:c.447A>G XP_011539469.1:p.Lys149=
XM_017000905.2:c.777A>G XP_016856394.1:p.Lys259=
NM_000147.5:c.1080A>G MANE Select NP_000138.2:p.Lys360=
NR_174379.1:n.1258A>G
NR_174380.1:n.1307A>G
NR_174381.1:n.1146A>G
NR_174382.1:n.1543A>G