Canonical Allele Identifier: CA2794592729
Gene: CDKN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718123_12718124insAAACACACCCAACA , CM000674.2:g.12718123_12718124insAAACACACCCAACA GRCh38
NC_000012.11:g.12871057_12871058insAAACACACCCAACA , CM000674.1:g.12871057_12871058insAAACACACCCAACA GRCh37
NC_000012.10:g.12762324_12762325insAAACACACCCAACA NCBI36
NG_016341.1:g.5756_5757insAAACACACCCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.284_285insAAACACACCCAACA ENSP00000507272.1:p.Lys96AsnfsTer28
ENST00000682620.1:n.1631-702_1631-701insAAACACACCCAACA
ENST00000684771.1:n.585-702_585-701insAAACACACCCAACA
ENST00000228872.9:c.284_285insAAACACACCCAACA MANE Select ENSP00000228872.4:p.Lys96AsnfsTer28
ENST00000228872.8:c.284_285insAAACACACCCAACA ENSP00000228872.4:p.Lys96AsnfsTer28
ENST00000396340.1:c.284_285insAAACACACCCAACA ENSP00000379629.1:p.Lys96AsnfsTer28
ENST00000442489.1:c.193+70_193+71insAAACACACCCAACA ENSP00000407597.1:n.193+70_193+71insAAACACACCCAACA
ENST00000477087.1:n.155-702_155-701insAAACACACCCAACA
NM_004064.4:c.284_285insAAACACACCCAACA NP_004055.1:p.Lys96AsnfsTer28
NM_004064.5:c.284_285insAAACACACCCAACA MANE Select NP_004055.1:p.Lys96AsnfsTer28