Canonical Allele Identifier: CA2580085163

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 2140529
• ClinVar RCV Id: RCV003073717

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717866_12717868del , CM000674.2:g.12717866_12717868del	GRCh38
NC_000012.11:g.12870800_12870802del , CM000674.1:g.12870800_12870802del	GRCh37
NC_000012.10:g.12762067_12762069del	NCBI36
NG_016341.1:g.5499_5501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.27_29del	ENSP00000507272.1:p.Ser10del
ENST00000682620.1:n.1631-959_1631-957del
ENST00000684771.1:n.585-959_585-957del
ENST00000228872.9:c.27_29del MANE Select	ENSP00000228872.4:p.Ser10del
ENST00000228872.8:c.27_29del	ENSP00000228872.4:p.Ser10del
ENST00000396340.1:c.27_29del	ENSP00000379629.1:p.Ser10del
ENST00000442489.1:c.6_8del	ENSP00000407597.1:p.Ser3del
ENST00000477087.1:n.155-959_155-957del
NM_004064.4:c.27_29del	NP_004055.1:p.Ser10del
NM_004064.5:c.27_29del MANE Select	NP_004055.1:p.Ser10del