Canonical Allele Identifier: CA2017047835

Gene: CDKN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718324_12718325delinsCT , CM000674.2:g.12718324_12718325delinsCT	GRCh38
NC_000012.11:g.12871258_12871259delinsCT , CM000674.1:g.12871258_12871259delinsCT	GRCh37
NC_000012.10:g.12762525_12762526delinsCT	NCBI36
NG_016341.1:g.5957_5958delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.475+10_475+11delinsCT	ENSP00000507272.1:n.475+10_475+11delinsCT
ENST00000682620.1:n.1631-501_1631-500delinsCT
ENST00000684771.1:n.585-501_585-500delinsCT
ENST00000228872.9:c.475+10_475+11delinsCT MANE Select	ENSP00000228872.4:n.475+10_475+11delinsCT
ENST00000228872.8:c.475+10_475+11delinsCT	ENSP00000228872.4:n.475+10_475+11delinsCT
ENST00000396340.1:c.475+10_475+11delinsCT	ENSP00000379629.1:n.475+10_475+11delinsCT
ENST00000442489.1:c.193+271_193+272delinsCT	ENSP00000407597.1:n.193+271_193+272delinsCT
ENST00000477087.1:n.155-501_155-500delinsCT
NM_004064.4:c.475+10_475+11delinsCT	NP_004055.1:n.475+10_475+11delinsCT
NM_004064.5:c.475+10_475+11delinsCT MANE Select	NP_004055.1:n.475+10_475+11delinsCT