Canonical Allele Identifier: CA340427260
Gene: CDCP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.54141326C>G , CM000663.2:g.54141326C>G GRCh38
NC_000001.10:g.54606999C>G , CM000663.1:g.54606999C>G GRCh37
NC_000001.9:g.54379587C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001353655.3:c.535G>C MANE Select NP_001340584.1:p.Gly179Arg
ENST00000530059.3:c.535G>C MANE Select ENSP00000489959.1:p.Gly179Arg
NM_001353655.1:c.535G>C NP_001340584.1:p.Gly179Arg
NM_001353655.2:c.535G>C NP_001340584.1:p.Gly179Arg
NM_201546.3:c.535G>C NP_963840.2:p.Gly179Arg
NM_201546.4:c.535G>C NP_963840.2:p.Gly179Arg
NM_201546.5:c.535G>C NP_963840.2:p.Gly179Arg
ENST00000371330.1:c.535G>C ENSP00000360381.1:p.Gly179Arg
ENST00000525949.1:n.445G>C
ENST00000530059.2:c.535G>C ENSP00000489959.1:p.Gly179Arg
ENST00000637610.1:c.*699G>C ENSP00000490901.1:n.*699G>C