Canonical Allele Identifier: CA566531967

Gene: CDKN1A

Linked Data

• dbSNP Id: rs1445659229
• gnomAD v2: 6-36653587-A-ATT
• MyVariant Identifiers: chr6:g.36653587_36653588insTT (hg19) ; chr6:g.36685810_36685811insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685810_36685811insTT , CM000668.2:g.36685810_36685811insTT	GRCh38
NC_000006.11:g.36653587_36653588insTT , CM000668.1:g.36653587_36653588insTT	GRCh37
NC_000006.10:g.36761565_36761566insTT	NCBI36
NG_009364.1:g.12129_12130insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.*10_*11insTT MANE Select	ENSP00000244741.6:n.*10_*11insTT
ENST00000244741.9:c.*10_*11insTT	ENSP00000244741.5:n.*10_*11insTT
ENST00000373711.3:c.*10_*11insTT	ENSP00000362815.1:n.*10_*11insTT
ENST00000405375.5:c.*10_*11insTT	ENSP00000384849.1:n.*10_*11insTT
ENST00000448526.6:c.*10_*11insTT	ENSP00000409259.3:n.*10_*11insTT
ENST00000615513.4:c.*10_*11insTT	ENSP00000482768.1:n.*10_*11insTT
NM_000389.4:c.*10_*11insTT	NP_000380.1:n.*10_*11insTT
NM_001220777.1:c.*10_*11insTT	NP_001207706.1:n.*10_*11insTT
NM_001220778.1:c.*10_*11insTT	NP_001207707.1:n.*10_*11insTT
NM_001291549.1:c.*10_*11insTT	NP_001278478.1:n.*10_*11insTT
NM_078467.2:c.*10_*11insTT	NP_510867.1:n.*10_*11insTT
NM_000389.5:c.*10_*11insTT MANE Select	NP_000380.1:n.*10_*11insTT
NM_001220777.2:c.*10_*11insTT	NP_001207706.1:n.*10_*11insTT
NM_001220778.2:c.*10_*11insTT	NP_001207707.1:n.*10_*11insTT
NM_001291549.3:c.*10_*11insTT	NP_001278478.1:n.*10_*11insTT
NM_001374509.1:c.*10_*11insTT	NP_001361438.1:n.*10_*11insTT
NM_001374510.1:c.*10_*11insTT	NP_001361439.1:n.*10_*11insTT
NM_001374511.1:c.*10_*11insTT	NP_001361440.1:n.*10_*11insTT
NM_001374512.1:c.*300_*301insTT	NP_001361441.1:n.*300_*301insTT
NM_001374513.1:c.*10_*11insTT	NP_001361442.1:n.*10_*11insTT
NM_078467.3:c.*10_*11insTT	NP_510867.1:n.*10_*11insTT