Canonical Allele Identifier: CA2277807811

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099529C= , CM000679.2:g.80099529C=	GRCh38
NC_000017.10:g.78073328C= , CM000679.1:g.78073328C=	GRCh37
NC_000017.9:g.75687923C=	NCBI36
NG_009822.1:g.2974C= , LRG_673:g.2974C=
NG_029761.1:g.67898C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.3183C= MANE Select	ENSP00000380679.4:p.Asn1061=
ENST00000397545.8:c.3183C=	ENSP00000380679.4:p.Asn1061=
ENST00000574799.5:n.2720C=
NM_017950.3:c.3183C=	NP_060420.2:p.Asn1061=
XM_011524963.1:c.3093C=	XP_011523265.1:p.Asn1031=
XM_011524964.1:c.2004C=	XP_011523266.1:p.Asn668=
XM_011524963.3:c.3093C=	XP_011523265.1:p.Asn1031=
XM_011524964.3:c.2004C=	XP_011523266.1:p.Asn668=
XM_024450821.1:c.3093C=	XP_024306589.1:p.Asn1031=
XR_934495.2:n.3301C=
NM_017950.4:c.3183C= MANE Select	NP_060420.2:p.Asn1061=