Canonical Allele Identifier: CA2697559113
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2695719
ClinVar RCV Id: RCV003509916

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718218dup , CM000674.2:g.12718218dup GRCh38
NC_000012.11:g.12871152dup , CM000674.1:g.12871152dup GRCh37
NC_000012.10:g.12762419dup NCBI36
NG_016341.1:g.5851dup

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.379dup ENSP00000507272.1:p.Asp127GlyfsTer10
ENST00000682620.1:n.1631-607dup
ENST00000684771.1:n.585-607dup
ENST00000228872.9:c.379dup MANE Select ENSP00000228872.4:p.Asp127GlyfsTer10
ENST00000228872.8:c.379dup ENSP00000228872.4:p.Asp127GlyfsTer10
ENST00000396340.1:c.379dup ENSP00000379629.1:p.Asp127GlyfsTer10
ENST00000442489.1:c.193+165dup ENSP00000407597.1:n.193+165dup
ENST00000477087.1:n.155-607dup
NM_004064.4:c.379dup NP_004055.1:p.Asp127GlyfsTer10
NM_004064.5:c.379dup MANE Select NP_004055.1:p.Asp127GlyfsTer10