Canonical Allele Identifier: CA1621456872

Gene: CDKN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36684112_36684113delinsCG , CM000668.2:g.36684112_36684113delinsCG	GRCh38
NC_000006.11:g.36651889_36651890delinsCG , CM000668.1:g.36651889_36651890delinsCG	GRCh37
NC_000006.10:g.36759867_36759868delinsCG	NCBI36
NG_009364.1:g.10431_10432delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.11_12delinsCG MANE Select	ENSP00000244741.6:p.Pro4=
ENST00000244741.9:c.11_12delinsCG	ENSP00000244741.5:p.Pro4=
ENST00000373711.3:c.11_12delinsCG	ENSP00000362815.1:p.Pro4=
ENST00000405375.5:c.11_12delinsCG	ENSP00000384849.1:p.Pro4=
ENST00000448526.6:c.11_12delinsCG	ENSP00000409259.3:p.Pro4=
ENST00000459970.1:n.205_206delinsCG
ENST00000478800.1:n.230_231delinsCG
ENST00000615513.4:c.11_12delinsCG	ENSP00000482768.1:p.Pro4=
NM_000389.4:c.11_12delinsCG	NP_000380.1:p.Pro4=
NM_001220777.1:c.11_12delinsCG	NP_001207706.1:p.Pro4=
NM_001220778.1:c.11_12delinsCG	NP_001207707.1:p.Pro4=
NM_001291549.1:c.113_114delinsCG	NP_001278478.1:p.Pro38=
NM_078467.2:c.11_12delinsCG	NP_510867.1:p.Pro4=
NM_000389.5:c.11_12delinsCG MANE Select	NP_000380.1:p.Pro4=
NM_001220777.2:c.11_12delinsCG	NP_001207706.1:p.Pro4=
NM_001220778.2:c.11_12delinsCG	NP_001207707.1:p.Pro4=
NM_001291549.3:c.113_114delinsCG	NP_001278478.1:p.Pro38=
NM_001374509.1:c.113_114delinsCG	NP_001361438.1:p.Pro38=
NM_001374510.1:c.50_51delinsCG	NP_001361439.1:p.Pro17=
NM_001374511.1:c.11_12delinsCG	NP_001361440.1:p.Pro4=
NM_001374512.1:c.11_12delinsCG	NP_001361441.1:p.Pro4=
NM_001374513.1:c.11_12delinsCG	NP_001361442.1:p.Pro4=
NM_078467.3:c.11_12delinsCG	NP_510867.1:p.Pro4=