Canonical Allele Identifier: CA186093
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs786201011

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718213_12718214del , CM000674.2:g.12718213_12718214del GRCh38
NC_000012.11:g.12871147_12871148del , CM000674.1:g.12871147_12871148del GRCh37
NC_000012.10:g.12762414_12762415del NCBI36
NG_016341.1:g.5846_5847del

Transcript Alleles

HGVS Amino-acid change
ENST00000228872.9:c.374_375del MANE Select ENSP00000228872.4:p.Ser125Ter
ENST00000228872.8:c.374_375del ENSP00000228872.4:p.Ser125Ter
ENST00000396340.1:c.374_375del ENSP00000379629.1:p.Ser125Ter
ENST00000442489.1:n.193+160_193+161del ENSP00000407597.1:p.=
ENST00000477087.1:n.155-612_155-611del
NM_004064.4:c.374_375del NP_004055.1:p.Ser125Ter
NM_004064.5:c.374_375del MANE Select NP_004055.1:p.Ser125Ter