Canonical Allele Identifier: CA2017048963

Gene: CDKN1B

Linked Data

• dbSNP Id: rs1946529720

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12720338_12720340del , CM000674.2:g.12720338_12720340del	GRCh38
NC_000012.11:g.12873272_12873274del , CM000674.1:g.12873272_12873274del	GRCh37
NC_000012.10:g.12764539_12764541del	NCBI36
NG_016341.1:g.7971_7973del

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.*1392_*1394del	ENSP00000507272.1:n.*1392_*1394del
ENST00000682620.1:n.1761-698_1761-696del
ENST00000684771.1:n.715-698_715-696del
ENST00000228872.9:c.*9-698_*9-696del MANE Select	ENSP00000228872.4:n.*9-698_*9-696del
ENST00000228872.8:c.*9-698_*9-696del	ENSP00000228872.4:n.*9-698_*9-696del
ENST00000396340.1:c.476-727_476-725del	ENSP00000379629.1:n.476-727_476-725del
ENST00000442489.1:c.324-698_324-696del	ENSP00000407597.1:n.324-698_324-696del
ENST00000477087.1:n.285-698_285-696del
NM_004064.4:c.*9-698_*9-696del	NP_004055.1:n.*9-698_*9-696del
NM_004064.5:c.*9-698_*9-696del MANE Select	NP_004055.1:n.*9-698_*9-696del