Canonical Allele Identifier: CA2678467271

Gene: CDKN1A

Linked Data

• dbSNP Id: rs2150315585
• gnomAD v4: 6-36685842-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685842T>C , CM000668.2:g.36685842T>C	GRCh38
NC_000006.11:g.36653619T>C , CM000668.1:g.36653619T>C	GRCh37
NC_000006.10:g.36761597T>C	NCBI36
NG_009364.1:g.12161T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000244741.10:c.*42T>C MANE Select	ENSP00000244741.6:n.*42T>C
ENST00000244741.9:c.*42T>C	ENSP00000244741.5:n.*42T>C
ENST00000373711.3:c.*42T>C	ENSP00000362815.1:n.*42T>C
ENST00000405375.5:c.*42T>C	ENSP00000384849.1:n.*42T>C
ENST00000448526.6:c.*42T>C	ENSP00000409259.3:n.*42T>C
ENST00000615513.4:c.*42T>C	ENSP00000482768.1:n.*42T>C
NM_000389.4:c.*42T>C	NP_000380.1:n.*42T>C
NM_001220777.1:c.*42T>C	NP_001207706.1:n.*42T>C
NM_001220778.1:c.*42T>C	NP_001207707.1:n.*42T>C
NM_001291549.1:c.*42T>C	NP_001278478.1:n.*42T>C
NM_078467.2:c.*42T>C	NP_510867.1:n.*42T>C
NM_000389.5:c.*42T>C MANE Select	NP_000380.1:n.*42T>C
NM_001220777.2:c.*42T>C	NP_001207706.1:n.*42T>C
NM_001220778.2:c.*42T>C	NP_001207707.1:n.*42T>C
NM_001291549.3:c.*42T>C	NP_001278478.1:n.*42T>C
NM_001374509.1:c.*42T>C	NP_001361438.1:n.*42T>C
NM_001374510.1:c.*42T>C	NP_001361439.1:n.*42T>C
NM_001374511.1:c.*42T>C	NP_001361440.1:n.*42T>C
NM_001374512.1:c.*332T>C	NP_001361441.1:n.*332T>C
NM_001374513.1:c.*42T>C	NP_001361442.1:n.*42T>C
NM_078467.3:c.*42T>C	NP_510867.1:n.*42T>C