Canonical Allele Identifier: CA186088
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 183391
ClinVar RCV Id: RCV000162205
dbSNP Id: rs786201007

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717898_12717916dup , CM000674.2:g.12717898_12717916dup GRCh38
NC_000012.11:g.12870832_12870850dup , CM000674.1:g.12870832_12870850dup GRCh37
NC_000012.10:g.12762099_12762117dup NCBI36
NG_016341.1:g.5531_5549dup

Transcript Alleles

HGVS Amino-acid change
ENST00000228872.9:c.59_77dup MANE Select ENSP00000228872.4:p.Ser27GlyfsTer?
ENST00000228872.8:c.59_77dup ENSP00000228872.4:p.Ser27GlyfsTer?
ENST00000396340.1:c.59_77dup ENSP00000379629.1:p.Ser27GlyfsTer?
ENST00000442489.1:n.38_56dup ENSP00000407597.1:p.Ser20GlyfsTer?
ENST00000477087.1:n.155-927_155-909dup
NM_004064.4:c.59_77dup NP_004055.1:p.Ser27GlyfsTer?
NM_004064.5:c.59_77dup MANE Select NP_004055.1:p.Ser27GlyfsTer?