Canonical Allele Identifier: CA416626747
Gene: FUCA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.24175144A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23848654A>T , CM000663.2:g.23848654A>T GRCh38
NC_000001.10:g.24175144A>T , CM000663.1:g.24175144A>T GRCh37
NC_000001.9:g.24047731A>T NCBI36
NG_013346.1:g.24716T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.1155T>A MANE Select ENSP00000363603.3:p.Ser385=
ENST00000374479.3:c.1155T>A ENSP00000363603.3:p.Ser385=
NM_000147.4:c.1155T>A NP_000138.2:p.Ser385=
XM_005245821.1:c.780T>A XP_005245878.1:p.Ser260=
XM_011541167.1:c.522T>A XP_011539469.1:p.Ser174=
XM_005245821.3:c.780T>A XP_005245878.1:p.Ser260=
XM_011541167.3:c.522T>A XP_011539469.1:p.Ser174=
XM_017000905.2:c.852T>A XP_016856394.1:p.Ser284=
NM_000147.5:c.1155T>A MANE Select NP_000138.2:p.Ser385=
NR_174379.1:n.1333T>A
NR_174380.1:n.1382T>A
NR_174381.1:n.1221T>A
NR_174382.1:n.1618T>A