Canonical Allele Identifier: CA416691229
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24194630C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23868140C>A , CM000663.2:g.23868140C>A GRCh38
NC_000001.10:g.24194630C>A , CM000663.1:g.24194630C>A GRCh37
NC_000001.9:g.24067217C>A NCBI36
NG_013346.1:g.5230G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.147G>T MANE Select ENSP00000363603.3:p.Leu49=
ENST00000374479.3:c.147G>T ENSP00000363603.3:p.Leu49=
NM_000147.4:c.147G>T NP_000138.2:p.Leu49=
XM_005245821.1:c.-403G>T XP_005245878.1:n.-403G>T
XM_005245821.3:c.-403G>T XP_005245878.1:n.-403G>T
NM_000147.5:c.147G>T MANE Select NP_000138.2:p.Leu49=
NR_174379.1:n.151G>T
NR_174380.1:n.151G>T
NR_174381.1:n.151G>T
NR_174382.1:n.151G>T