Canonical Allele Identifier: CA2277807813

Gene: CCDC40

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80099531T= , CM000679.2:g.80099531T=	GRCh38
NC_000017.10:g.78073330T= , CM000679.1:g.78073330T=	GRCh37
NC_000017.9:g.75687925T=	NCBI36
NG_009822.1:g.2976T= , LRG_673:g.2976T=
NG_029761.1:g.67900T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.3185T= MANE Select	ENSP00000380679.4:p.Leu1062=
ENST00000397545.8:c.3185T=	ENSP00000380679.4:p.Leu1062=
ENST00000574799.5:n.2722T=
NM_017950.3:c.3185T=	NP_060420.2:p.Leu1062=
XM_011524963.1:c.3095T=	XP_011523265.1:p.Leu1032=
XM_011524964.1:c.2006T=	XP_011523266.1:p.Leu669=
XM_011524963.3:c.3095T=	XP_011523265.1:p.Leu1032=
XM_011524964.3:c.2006T=	XP_011523266.1:p.Leu669=
XM_024450821.1:c.3095T=	XP_024306589.1:p.Leu1032=
XR_934495.2:n.3303T=
NM_017950.4:c.3185T= MANE Select	NP_060420.2:p.Leu1062=