Canonical Allele Identifier: CA2617686057

Gene: CDKN1B

Linked Data

• gnomAD v4: 12-12718190-TTTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12718193_12718196del , CM000674.2:g.12718193_12718196del	GRCh38
NC_000012.11:g.12871127_12871130del , CM000674.1:g.12871127_12871130del	GRCh37
NC_000012.10:g.12762394_12762397del	NCBI36
NG_016341.1:g.5826_5829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.354_357del	ENSP00000507272.1:p.Ile119GlyfsTer25
ENST00000682620.1:n.1631-632_1631-629del
ENST00000684771.1:n.585-632_585-629del
ENST00000228872.9:c.354_357del MANE Select	ENSP00000228872.4:p.Ile119GlyfsTer25
ENST00000228872.8:c.354_357del	ENSP00000228872.4:p.Ile119GlyfsTer25
ENST00000396340.1:c.354_357del	ENSP00000379629.1:p.Ile119GlyfsTer25
ENST00000442489.1:c.193+140_193+143del	ENSP00000407597.1:n.193+140_193+143del
ENST00000477087.1:n.155-632_155-629del
NM_004064.4:c.354_357del	NP_004055.1:p.Ile119GlyfsTer25
NM_004064.5:c.354_357del MANE Select	NP_004055.1:p.Ile119GlyfsTer25