Canonical Allele Identifier: CA363834749

Gene: CDKN1A

Linked Data

• dbSNP Id: rs2150315391
• MyVariant Identifiers: chr6:g.36653531T>C (hg19) ; chr6:g.36685754T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36685754T>C , CM000668.2:g.36685754T>C	GRCh38
NC_000006.11:g.36653531T>C , CM000668.1:g.36653531T>C	GRCh37
NC_000006.10:g.36761509T>C	NCBI36
NG_009364.1:g.12073T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000244741.10:c.449T>C MANE Select	ENSP00000244741.6:p.Phe150Ser
ENST00000244741.9:c.449T>C	ENSP00000244741.5:p.Phe150Ser
ENST00000373711.3:c.449T>C	ENSP00000362815.1:p.Phe150Ser
ENST00000405375.5:c.449T>C	ENSP00000384849.1:p.Phe150Ser
ENST00000448526.6:c.449T>C	ENSP00000409259.3:p.Phe150Ser
ENST00000615513.4:c.449T>C	ENSP00000482768.1:p.Phe150Ser
NM_000389.4:c.449T>C	NP_000380.1:p.Phe150Ser
NM_001220777.1:c.449T>C	NP_001207706.1:p.Phe150Ser
NM_001220778.1:c.449T>C	NP_001207707.1:p.Phe150Ser
NM_001291549.1:c.551T>C	NP_001278478.1:p.Phe184Ser
NM_078467.2:c.449T>C	NP_510867.1:p.Phe150Ser
NM_000389.5:c.449T>C MANE Select	NP_000380.1:p.Phe150Ser
NM_001220777.2:c.449T>C	NP_001207706.1:p.Phe150Ser
NM_001220778.2:c.449T>C	NP_001207707.1:p.Phe150Ser
NM_001291549.3:c.551T>C	NP_001278478.1:p.Phe184Ser
NM_001374509.1:c.551T>C	NP_001361438.1:p.Phe184Ser
NM_001374510.1:c.488T>C	NP_001361439.1:p.Phe163Ser
NM_001374511.1:c.548T>C	NP_001361440.1:p.Phe183Ser
NM_001374512.1:c.*244T>C	NP_001361441.1:n.*244T>C
NM_001374513.1:c.449T>C	NP_001361442.1:p.Phe150Ser
NM_078467.3:c.449T>C	NP_510867.1:p.Phe150Ser