Canonical Allele Identifier: CA2017049031
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12720500_12720504delinsGAAAA , CM000674.2:g.12720500_12720504delinsGAAAA GRCh38
NC_000012.11:g.12873434_12873438delinsGAAAA , CM000674.1:g.12873434_12873438delinsGAAAA GRCh37
NC_000012.10:g.12764701_12764705delinsGAAAA NCBI36
NG_016341.1:g.8133_8137delinsGAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.*1554_*1558delinsGAAAA ENSP00000507272.1:n.*1554_*1558delinsGAAAA
ENST00000682620.1:n.1761-536_1761-532delinsGAAAA
ENST00000684771.1:n.715-536_715-532delinsGAAAA
ENST00000228872.9:c.*9-536_*9-532delinsGAAAA MANE Select ENSP00000228872.4:n.*9-536_*9-532delinsGAAAA
ENST00000228872.8:c.*9-536_*9-532delinsGAAAA ENSP00000228872.4:n.*9-536_*9-532delinsGAAAA
ENST00000396340.1:c.476-565_476-561delinsGAAAA ENSP00000379629.1:n.476-565_476-561delinsGAAAA
ENST00000442489.1:c.324-536_324-532delinsGAAAA ENSP00000407597.1:n.324-536_324-532delinsGAAAA
ENST00000477087.1:n.285-536_285-532delinsGAAAA
NM_004064.4:c.*9-536_*9-532delinsGAAAA NP_004055.1:n.*9-536_*9-532delinsGAAAA
NM_004064.5:c.*9-536_*9-532delinsGAAAA MANE Select NP_004055.1:n.*9-536_*9-532delinsGAAAA