Canonical Allele Identifier: CA782407395

Gene: CNDP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.74520377C>G , CM000680.2:g.74520377C>G	GRCh38
NC_000018.9:g.72187612C>G , CM000680.1:g.72187612C>G	GRCh37
NC_000018.8:g.70338592C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324262.9:c.*309C>G MANE Select	ENSP00000325548.4:n.*309C>G
ENST00000324262.8:c.*309C>G	ENSP00000325548.4:n.*309C>G
ENST00000324301.12:c.*309C>G	ENSP00000325756.8:n.*309C>G
ENST00000579624.1:c.449C>G	ENSP00000462034.1:n.449C>G
ENST00000579847.5:c.*309C>G	ENSP00000462311.1:n.*309C>G
ENST00000584581.5:n.3779C>G
NM_001168499.1:c.*309C>G	NP_001161971.1:n.*309C>G
NM_018235.2:c.*309C>G	NP_060705.2:n.*309C>G
XM_005266728.1:c.*309C>G	XP_005266785.1:n.*309C>G
XM_006722503.1:c.*309C>G	XP_006722566.1:n.*309C>G
XM_011526071.1:c.*309C>G	XP_011524373.1:n.*309C>G
XM_011526072.1:c.*309C>G	XP_011524374.1:n.*309C>G
XM_011526073.1:c.*309C>G	XP_011524375.1:n.*309C>G
XM_005266728.3:c.*309C>G	XP_005266785.1:n.*309C>G
XM_006722503.2:c.*309C>G	XP_006722566.1:n.*309C>G
XM_011526072.2:c.*309C>G	XP_011524374.1:n.*309C>G
XM_011526073.3:c.*309C>G	XP_011524375.1:n.*309C>G
NM_018235.3:c.*309C>G MANE Select	NP_060705.2:n.*309C>G
NM_001370248.1:c.*309C>G	NP_001357177.1:n.*309C>G
NM_001370249.1:c.*309C>G	NP_001357178.1:n.*309C>G
NM_001370250.1:c.*309C>G	NP_001357179.1:n.*309C>G
NM_001370254.1:c.*309C>G	NP_001357183.1:n.*309C>G
NM_001168499.2:c.*309C>G	NP_001161971.1:n.*309C>G