Canonical Allele Identifier: CA1087900129
Gene: CDKN1A HGNC NCBI

Linked Data

dbSNP Id: rs1761926299

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36681132del , CM000668.2:g.36681132del GRCh38
NC_000006.11:g.36648909del , CM000668.1:g.36648909del GRCh37
NC_000006.10:g.36756887del NCBI36
NG_009364.1:g.7451del

Transcript Alleles

HGVS Amino-acid change
ENST00000244741.10:c.-6+2334del MANE Select ENSP00000244741.6:n.-6+2334del
ENST00000244741.9:c.-6+2334del ENSP00000244741.5:n.-6+2334del
ENST00000373711.3:c.-96-1508del ENSP00000362815.1:n.-96-1508del
ENST00000405375.5:c.-6+2193del ENSP00000384849.1:n.-6+2193del
ENST00000448526.6:c.-5-2965del ENSP00000409259.3:n.-5-2965del
ENST00000459970.1:n.190-2965del
ENST00000478800.1:n.214+2193del
ENST00000615513.4:c.-5-2965del ENSP00000482768.1:n.-5-2965del
NM_000389.4:c.-6+2334del NP_000380.1:n.-6+2334del
NM_001220777.1:c.-5-2965del NP_001207706.1:n.-5-2965del
NM_001220778.1:c.-6+2193del NP_001207707.1:n.-6+2193del
NM_001291549.1:c.98-2965del NP_001278478.1:n.98-2965del
NM_078467.2:c.-5-2965del NP_510867.1:n.-5-2965del
XM_011515041.1:c.*278del XP_011513343.1:n.*278del
NM_000389.5:c.-6+2334del MANE Select NP_000380.1:n.-6+2334del
NM_001220777.2:c.-5-2965del NP_001207706.1:n.-5-2965del
NM_001220778.2:c.-6+2193del NP_001207707.1:n.-6+2193del
NM_001291549.3:c.98-2965del NP_001278478.1:n.98-2965del
NM_001374509.1:c.98-2965del NP_001361438.1:n.98-2965del
NM_001374510.1:c.35-2965del NP_001361439.1:n.35-2965del
NM_001374511.1:c.-6+2334del NP_001361440.1:n.-6+2334del
NM_001374512.1:c.-6+2334del NP_001361441.1:n.-6+2334del
NM_001374513.1:c.-6+2227del NP_001361442.1:n.-6+2227del
NM_078467.3:c.-5-2965del NP_510867.1:n.-5-2965del