Canonical Allele Identifier: CA2695216100
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718119_12718120delinsG , CM000674.2:g.12718119_12718120delinsG GRCh38
NC_000012.11:g.12871053_12871054delinsG , CM000674.1:g.12871053_12871054delinsG GRCh37
NC_000012.10:g.12762320_12762321delinsG NCBI36
NG_016341.1:g.5752_5753delinsG

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.280_281delinsG ENSP00000507272.1:p.Pro94AlafsTer25
ENST00000682620.1:n.1631-706_1631-705delinsG
ENST00000684771.1:n.585-706_585-705delinsG
ENST00000228872.9:c.280_281delinsG MANE Select ENSP00000228872.4:p.Pro94AlafsTer25
ENST00000228872.8:c.280_281delinsG ENSP00000228872.4:p.Pro94AlafsTer25
ENST00000396340.1:c.280_281delinsG ENSP00000379629.1:p.Pro94AlafsTer25
ENST00000442489.1:c.193+66_193+67delinsG ENSP00000407597.1:n.193+66_193+67delinsG
ENST00000477087.1:n.155-706_155-705delinsG
NM_004064.4:c.280_281delinsG NP_004055.1:p.Pro94AlafsTer25
NM_004064.5:c.280_281delinsG MANE Select NP_004055.1:p.Pro94AlafsTer25