Canonical Allele Identifier: CA2314100425
Gene: CNDP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.74522015C= , CM000680.2:g.74522015C= GRCh38
NC_000018.9:g.72189250C= , CM000680.1:g.72189250C= GRCh37
NC_000018.8:g.70340230C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_018235.3:c.*1947C= MANE Select NP_060705.2:n.*1947C=
ENST00000324262.9:c.*1947C= MANE Select ENSP00000325548.4:n.*1947C=
NM_001168499.1:c.*1947C= NP_001161971.1:n.*1947C=
NM_001168499.2:c.*1947C= NP_001161971.1:n.*1947C=
NM_001370248.1:c.*1947C= NP_001357177.1:n.*1947C=
NM_001370249.1:c.*1947C= NP_001357178.1:n.*1947C=
NM_001370250.1:c.*1947C= NP_001357179.1:n.*1947C=
NM_001370254.1:c.*1947C= NP_001357183.1:n.*1947C=
NM_018235.2:c.*1947C= NP_060705.2:n.*1947C=
ENST00000324262.8:c.*1947C= ENSP00000325548.4:n.*1947C=