Canonical Allele Identifier: CA1621457068

Gene: CDKN1A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.36684517G= , CM000668.2:g.36684517G=	GRCh38
NC_000006.11:g.36652294G= , CM000668.1:g.36652294G=	GRCh37
NC_000006.10:g.36760272G=	NCBI36
NG_009364.1:g.10836G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244741.10:c.416G= MANE Select	ENSP00000244741.6:p.Gly139=
ENST00000244741.9:c.416G=	ENSP00000244741.5:p.Gly139=
ENST00000373711.3:c.416G=	ENSP00000362815.1:p.Gly139=
ENST00000405375.5:c.416G=	ENSP00000384849.1:p.Gly139=
ENST00000448526.6:c.416G=	ENSP00000409259.3:p.Gly139=
ENST00000615513.4:c.416G=	ENSP00000482768.1:p.Gly139=
NM_000389.4:c.416G=	NP_000380.1:p.Gly139=
NM_001220777.1:c.416G=	NP_001207706.1:p.Gly139=
NM_001220778.1:c.416G=	NP_001207707.1:p.Gly139=
NM_001291549.1:c.518G=	NP_001278478.1:p.Gly173=
NM_078467.2:c.416G=	NP_510867.1:p.Gly139=
NM_000389.5:c.416G= MANE Select	NP_000380.1:p.Gly139=
NM_001220777.2:c.416G=	NP_001207706.1:p.Gly139=
NM_001220778.2:c.416G=	NP_001207707.1:p.Gly139=
NM_001291549.3:c.518G=	NP_001278478.1:p.Gly173=
NM_001374509.1:c.518G=	NP_001361438.1:p.Gly173=
NM_001374510.1:c.455G=	NP_001361439.1:p.Gly152=
NM_001374511.1:c.416G=	NP_001361440.1:p.Gly139=
NM_001374512.1:c.416G=	NP_001361441.1:p.Gly139=
NM_001374513.1:c.416G=	NP_001361442.1:p.Gly139=
NM_078467.3:c.416G=	NP_510867.1:p.Gly139=