Canonical Allele Identifier: CA2580615136

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 1784392
• ClinVar RCV Id: RCV002417329

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718040_12718041del , CM000674.2:g.12718040_12718041del	GRCh38
NC_000012.11:g.12870974_12870975del , CM000674.1:g.12870974_12870975del	GRCh37
NC_000012.10:g.12762241_12762242del	NCBI36
NG_016341.1:g.5673_5674del

Transcript Alleles

HGVS	Amino-acid change
ENST00000614874.2:c.201_202del	ENSP00000507272.1:p.His67GlnfsTer?
ENST00000682620.1:n.1631-785_1631-784del
ENST00000684771.1:n.585-785_585-784del
ENST00000228872.9:c.201_202del MANE Select	ENSP00000228872.4:p.His67GlnfsTer?
ENST00000228872.8:c.201_202del	ENSP00000228872.4:p.His67GlnfsTer?
ENST00000396340.1:c.201_202del	ENSP00000379629.1:p.His67GlnfsTer?
ENST00000442489.1:c.180_181del	ENSP00000407597.1:p.His60GlnfsTer?
ENST00000477087.1:n.155-785_155-784del
NM_004064.4:c.201_202del	NP_004055.1:p.His67GlnfsTer?
NM_004064.5:c.201_202del MANE Select	NP_004055.1:p.His67GlnfsTer?