Canonical Allele Identifier: CA401350882

Gene: CCDC40

Linked Data

• MyVariant Identifiers: chr17:g.78063586A>G (hg19) ; chr17:g.80089787A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.80089787A>G , CM000679.2:g.80089787A>G	GRCh38
NC_000017.10:g.78063586A>G , CM000679.1:g.78063586A>G	GRCh37
NC_000017.9:g.75678181A>G	NCBI36
NG_029761.1:g.58156A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000397545.9:c.2735A>G MANE Select	ENSP00000380679.4:p.Lys912Arg
ENST00000374877.7:c.2735A>G	ENSP00000364011.3:p.Lys912Arg
ENST00000397545.8:c.2735A>G	ENSP00000380679.4:p.Lys912Arg
ENST00000572253.5:n.2986A>G
ENST00000573903.1:n.397A>G
ENST00000574799.5:n.2272A>G
ENST00000575431.1:n.379A>G
NM_001243342.1:c.2735A>G	NP_001230271.1:p.Lys912Arg
NM_017950.3:c.2735A>G	NP_060420.2:p.Lys912Arg
XM_011524963.1:c.2645A>G	XP_011523265.1:p.Lys882Arg
XM_011524964.1:c.1556A>G	XP_011523266.1:p.Lys519Arg
XR_934495.1:n.2853A>G
XM_011524963.3:c.2645A>G	XP_011523265.1:p.Lys882Arg
XM_011524964.3:c.1556A>G	XP_011523266.1:p.Lys519Arg
XM_024450821.1:c.2645A>G	XP_024306589.1:p.Lys882Arg
XR_934495.2:n.2853A>G
NM_017950.4:c.2735A>G MANE Select	NP_060420.2:p.Lys912Arg
NM_001243342.2:c.2735A>G	NP_001230271.1:p.Lys912Arg