Canonical Allele Identifier: CA2067835331

Gene: ANAPC5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121318348G= , CM000674.2:g.121318348G=	GRCh38
NC_000012.11:g.121756151G= , CM000674.1:g.121756151G=	GRCh37
NC_000012.10:g.120240534G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261819.8:c.1822C= MANE Select	ENSP00000261819.3:p.Leu608=
ENST00000261819.7:c.1822C=	ENSP00000261819.3:p.Leu608=
ENST00000441917.6:c.1486C=	ENSP00000415061.2:p.Leu496=
ENST00000534976.5:n.2554C=
ENST00000535482.1:c.820C=	ENSP00000438754.1:p.Leu274=
ENST00000535641.5:n.2033C=
ENST00000539079.5:c.1146C=
ENST00000541887.5:c.1783C=	ENSP00000439875.1:p.Leu595=
ENST00000544314.5:n.940C=
ENST00000545218.5:n.992C=
NM_001137559.1:c.1486C=	NP_001131031.1:p.Leu496=
NM_016237.4:c.1822C=	NP_057321.2:p.Leu608=
XM_005253900.2:c.1783C=	XP_005253957.1:p.Leu595=
XM_006719449.1:c.628C=	XP_006719512.1:p.Leu210=
NM_001330489.1:c.1783C=	NP_001317418.1:p.Leu595=
XM_017019423.2:c.628C=	XP_016874912.1:p.Leu210=
XM_017019424.2:c.628C=	XP_016874913.1:p.Leu210=
NM_016237.5:c.1822C= MANE Select	NP_057321.2:p.Leu608=
NM_001330489.2:c.1783C=	NP_001317418.1:p.Leu595=