Canonical Allele Identifier: CA416691152
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24194489G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23867999G>A , CM000663.2:g.23867999G>A GRCh38
NC_000001.10:g.24194489G>A , CM000663.1:g.24194489G>A GRCh37
NC_000001.9:g.24067076G>A NCBI36
NG_013346.1:g.5371C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.288C>T MANE Select ENSP00000363603.3:p.Asn96=
ENST00000374479.3:c.288C>T ENSP00000363603.3:p.Asn96=
NM_000147.4:c.288C>T NP_000138.2:p.Asn96=
XM_005245821.1:c.-262C>T XP_005245878.1:n.-262C>T
XM_005245821.3:c.-262C>T XP_005245878.1:n.-262C>T
NM_000147.5:c.288C>T MANE Select NP_000138.2:p.Asn96=
NR_174379.1:n.292C>T
NR_174380.1:n.292C>T
NR_174381.1:n.292C>T
NR_174382.1:n.292C>T