Canonical Allele Identifier: CA2314099669

Gene: CNDP2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.74521136A= , CM000680.2:g.74521136A=	GRCh38
NC_000018.9:g.72188371A= , CM000680.1:g.72188371A=	GRCh37
NC_000018.8:g.70339351A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018235.3:c.*1068A= MANE Select	NP_060705.2:n.*1068A=
ENST00000324262.9:c.*1068A= MANE Select	ENSP00000325548.4:n.*1068A=
NM_001168499.1:c.*1068A=	NP_001161971.1:n.*1068A=
NM_001168499.2:c.*1068A=	NP_001161971.1:n.*1068A=
NM_001370248.1:c.*1068A=	NP_001357177.1:n.*1068A=
NM_001370249.1:c.*1068A=	NP_001357178.1:n.*1068A=
NM_001370250.1:c.*1068A=	NP_001357179.1:n.*1068A=
NM_001370254.1:c.*1068A=	NP_001357183.1:n.*1068A=
NM_018235.2:c.*1068A=	NP_060705.2:n.*1068A=
ENST00000324262.8:c.*1068A=	ENSP00000325548.4:n.*1068A=