Canonical Allele Identifier: CA2277807815

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099535A= , CM000679.2:g.80099535A=	GRCh38
NC_000017.10:g.78073334A= , CM000679.1:g.78073334A=	GRCh37
NC_000017.9:g.75687929A=	NCBI36
NG_009822.1:g.2980A= , LRG_673:g.2980A=
NG_029761.1:g.67904A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.3189A= MANE Select	ENSP00000380679.4:p.Ser1063=
ENST00000397545.8:c.3189A=	ENSP00000380679.4:p.Ser1063=
ENST00000574799.5:n.2726A=
NM_017950.3:c.3189A=	NP_060420.2:p.Ser1063=
XM_011524963.1:c.3099A=	XP_011523265.1:p.Ser1033=
XM_011524964.1:c.2010A=	XP_011523266.1:p.Ser670=
XM_011524963.3:c.3099A=	XP_011523265.1:p.Ser1033=
XM_011524964.3:c.2010A=	XP_011523266.1:p.Ser670=
XM_024450821.1:c.3099A=	XP_024306589.1:p.Ser1033=
XR_934495.2:n.3307A=
NM_017950.4:c.3189A= MANE Select	NP_060420.2:p.Ser1063=