Canonical Allele Identifier: CA2017048962

Gene: CDKN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12720335_12720338delinsATAT , CM000674.2:g.12720335_12720338delinsATAT	GRCh38
NC_000012.11:g.12873269_12873272delinsATAT , CM000674.1:g.12873269_12873272delinsATAT	GRCh37
NC_000012.10:g.12764536_12764539delinsATAT	NCBI36
NG_016341.1:g.7968_7971delinsATAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.*1389_*1392delinsATAT	ENSP00000507272.1:n.*1389_*1392delinsATAT...
ENST00000682620.1:n.1761-701_1761-698delinsATAT
ENST00000684771.1:n.715-701_715-698delinsATAT
ENST00000228872.9:c.*9-701_*9-698delinsATAT MANE Select	ENSP00000228872.4:n.*9-701_*9-698delinsAT...
ENST00000228872.8:c.*9-701_*9-698delinsATAT	ENSP00000228872.4:n.*9-701_*9-698delinsAT...
ENST00000396340.1:c.476-730_476-727delinsATAT	ENSP00000379629.1:n.476-730_476-727delins...
ENST00000442489.1:c.324-701_324-698delinsATAT	ENSP00000407597.1:n.324-701_324-698delins...
ENST00000477087.1:n.285-701_285-698delinsATAT
NM_004064.4:c.*9-701_*9-698delinsATAT	NP_004055.1:n.*9-701_*9-698delinsATAT
NM_004064.5:c.*9-701_*9-698delinsATAT MANE Select	NP_004055.1:n.*9-701_*9-698delinsATAT