Canonical Allele Identifier: CA2617685678

Gene: CDKN1B

Linked Data

• gnomAD v4: 12-12718044-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718044_12718045insT , CM000674.2:g.12718044_12718045insT	GRCh38
NC_000012.11:g.12870978_12870979insT , CM000674.1:g.12870978_12870979insT	GRCh37
NC_000012.10:g.12762245_12762246insT	NCBI36
NG_016341.1:g.5677_5678insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.205_206insT	ENSP00000507272.1:p.Pro69LeufsTer?
ENST00000682620.1:n.1631-781_1631-780insT
ENST00000684771.1:n.585-781_585-780insT
ENST00000228872.9:c.205_206insT MANE Select	ENSP00000228872.4:p.Pro69LeufsTer?
ENST00000228872.8:c.205_206insT	ENSP00000228872.4:p.Pro69LeufsTer?
ENST00000396340.1:c.205_206insT	ENSP00000379629.1:p.Pro69LeufsTer?
ENST00000442489.1:c.184_185insT	ENSP00000407597.1:p.Pro62LeufsTer?
ENST00000477087.1:n.155-781_155-780insT
NM_004064.4:c.205_206insT	NP_004055.1:p.Pro69LeufsTer?
NM_004064.5:c.205_206insT MANE Select	NP_004055.1:p.Pro69LeufsTer?