Canonical Allele Identifier: CA302782902

Gene: CNDP2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.74521017A>C , CM000680.2:g.74521017A>C	GRCh38
NC_000018.9:g.72188252A>C , CM000680.1:g.72188252A>C	GRCh37
NC_000018.8:g.70339232A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324262.9:c.*949A>C MANE Select	ENSP00000325548.4:n.*949A>C
ENST00000324262.8:c.*949A>C	ENSP00000325548.4:n.*949A>C
ENST00000324301.12:c.*949A>C	ENSP00000325756.8:n.*949A>C
ENST00000579624.1:c.1089A>C	ENSP00000462034.1:n.1089A>C
ENST00000579847.5:c.*949A>C	ENSP00000462311.1:n.*949A>C
ENST00000584581.5:n.4419A>C
NM_001168499.1:c.*949A>C	NP_001161971.1:n.*949A>C
NM_018235.2:c.*949A>C	NP_060705.2:n.*949A>C
XM_005266728.1:c.*949A>C	XP_005266785.1:n.*949A>C
XM_006722503.1:c.*949A>C	XP_006722566.1:n.*949A>C
XM_011526071.1:c.*949A>C	XP_011524373.1:n.*949A>C
XM_011526072.1:c.*949A>C	XP_011524374.1:n.*949A>C
XM_011526073.1:c.*949A>C	XP_011524375.1:n.*949A>C
XM_005266728.3:c.*949A>C	XP_005266785.1:n.*949A>C
XM_006722503.2:c.*949A>C	XP_006722566.1:n.*949A>C
XM_011526072.2:c.*949A>C	XP_011524374.1:n.*949A>C
XM_011526073.3:c.*949A>C	XP_011524375.1:n.*949A>C
NM_018235.3:c.*949A>C MANE Select	NP_060705.2:n.*949A>C
NM_001370248.1:c.*949A>C	NP_001357177.1:n.*949A>C
NM_001370249.1:c.*949A>C	NP_001357178.1:n.*949A>C
NM_001370250.1:c.*949A>C	NP_001357179.1:n.*949A>C
NM_001370254.1:c.*949A>C	NP_001357183.1:n.*949A>C
NM_001168499.2:c.*949A>C	NP_001161971.1:n.*949A>C