Canonical Allele Identifier: CA2017047954

Gene: CDKN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718473_12718477delinsCTGTT , CM000674.2:g.12718473_12718477delinsCTGTT	GRCh38
NC_000012.11:g.12871407_12871411delinsCTGTT , CM000674.1:g.12871407_12871411delinsCTGTT	GRCh37
NC_000012.10:g.12762674_12762678delinsCTGTT	NCBI36
NG_016341.1:g.6106_6110delinsCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.475+159_475+163delinsCTGTT	ENSP00000507272.1:n.475+159_475+163delinsCTGTT
ENST00000682620.1:n.1631-352_1631-348delinsCTGTT
ENST00000684771.1:n.585-352_585-348delinsCTGTT
ENST00000228872.9:c.475+159_475+163delinsCTGTT MANE Select	ENSP00000228872.4:n.475+159_475+163delinsCTGTT
ENST00000228872.8:c.475+159_475+163delinsCTGTT	ENSP00000228872.4:n.475+159_475+163delinsCTGTT
ENST00000396340.1:c.475+159_475+163delinsCTGTT	ENSP00000379629.1:n.475+159_475+163delinsCTGTT
ENST00000442489.1:c.194-352_194-348delinsCTGTT	ENSP00000407597.1:n.194-352_194-348delinsCTGTT
ENST00000477087.1:n.155-352_155-348delinsCTGTT
NM_004064.4:c.475+159_475+163delinsCTGTT	NP_004055.1:n.475+159_475+163delinsCTGTT
NM_004064.5:c.475+159_475+163delinsCTGTT MANE Select	NP_004055.1:n.475+159_475+163delinsCTGTT