Canonical Allele Identifier: CA1158990191
Gene: FUCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23865620A= , CM000663.2:g.23865620A= GRCh38
NC_000001.10:g.24192110A= , CM000663.1:g.24192110A= GRCh37
NC_000001.9:g.24064697A= NCBI36
NG_013346.1:g.7750T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374479.4:c.395T= MANE Select ENSP00000363603.3:p.Val132=
ENST00000374479.3:c.395T= ENSP00000363603.3:p.Val132=
NM_000147.4:c.395T= NP_000138.2:p.Val132=
XM_005245821.1:c.20T= XP_005245878.1:p.Val7=
XM_011541167.1:c.-239T= XP_011539469.1:n.-239T=
XM_005245821.3:c.20T= XP_005245878.1:p.Val7=
XM_011541167.3:c.-239T= XP_011539469.1:n.-239T=
XM_017000905.2:c.92T= XP_016856394.1:p.Val31=
NM_000147.5:c.395T= MANE Select NP_000138.2:p.Val132=
NR_174379.1:n.573T=
NR_174380.1:n.622T=
NR_174381.1:n.461T=
NR_174382.1:n.858T=