Canonical Allele Identifier: CA1621457049
Gene: CDKN1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.36684472G= , CM000668.2:g.36684472G= GRCh38
NC_000006.11:g.36652249G= , CM000668.1:g.36652249G= GRCh37
NC_000006.10:g.36760227G= NCBI36
NG_009364.1:g.10791G=

Transcript Alleles

HGVS Amino-acid change
ENST00000244741.10:c.371G= MANE Select ENSP00000244741.6:p.Gly124=
ENST00000244741.9:c.371G= ENSP00000244741.5:p.Gly124=
ENST00000373711.3:c.371G= ENSP00000362815.1:p.Gly124=
ENST00000405375.5:c.371G= ENSP00000384849.1:p.Gly124=
ENST00000448526.6:c.371G= ENSP00000409259.3:p.Gly124=
ENST00000459970.1:n.565G=
ENST00000478800.1:n.590G=
ENST00000615513.4:c.371G= ENSP00000482768.1:p.Gly124=
NM_000389.4:c.371G= NP_000380.1:p.Gly124=
NM_001220777.1:c.371G= NP_001207706.1:p.Gly124=
NM_001220778.1:c.371G= NP_001207707.1:p.Gly124=
NM_001291549.1:c.473G= NP_001278478.1:p.Gly158=
NM_078467.2:c.371G= NP_510867.1:p.Gly124=
NM_000389.5:c.371G= MANE Select NP_000380.1:p.Gly124=
NM_001220777.2:c.371G= NP_001207706.1:p.Gly124=
NM_001220778.2:c.371G= NP_001207707.1:p.Gly124=
NM_001291549.3:c.473G= NP_001278478.1:p.Gly158=
NM_001374509.1:c.473G= NP_001361438.1:p.Gly158=
NM_001374510.1:c.410G= NP_001361439.1:p.Gly137=
NM_001374511.1:c.371G= NP_001361440.1:p.Gly124=
NM_001374512.1:c.371G= NP_001361441.1:p.Gly124=
NM_001374513.1:c.371G= NP_001361442.1:p.Gly124=
NM_078467.3:c.371G= NP_510867.1:p.Gly124=