Canonical Allele Identifier: CA2314099670
Gene: CNDP2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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