Canonical Allele Identifier: CA2617685429

Gene: CDKN1B

Linked Data

• gnomAD v4: 12-12717860-TAACGGGAGCCCTAGCCTGGAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717861_12717882del , CM000674.2:g.12717861_12717882del	GRCh38
NC_000012.11:g.12870795_12870816del , CM000674.1:g.12870795_12870816del	GRCh37
NC_000012.10:g.12762062_12762083del	NCBI36
NG_016341.1:g.5494_5515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.22_43del	ENSP00000507272.1:p.Asn8GlyfsTer27
ENST00000682620.1:n.1631-964_1631-943del
ENST00000684771.1:n.585-964_585-943del
ENST00000228872.9:c.22_43del MANE Select	ENSP00000228872.4:p.Asn8GlyfsTer27
ENST00000228872.8:c.22_43del	ENSP00000228872.4:p.Asn8GlyfsTer27
ENST00000396340.1:c.22_43del	ENSP00000379629.1:p.Asn8GlyfsTer27
ENST00000442489.1:c.1_22del	ENSP00000407597.1:p.Asn1GlyfsTer27
ENST00000477087.1:n.155-964_155-943del
NM_004064.4:c.22_43del	NP_004055.1:p.Asn8GlyfsTer27
NM_004064.5:c.22_43del MANE Select	NP_004055.1:p.Asn8GlyfsTer27