Canonical Allele Identifier: CA913686164
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

dbSNP Id: rs1565419168

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717712_12717713del , CM000674.2:g.12717712_12717713del GRCh38
NC_000012.11:g.12870646_12870647del , CM000674.1:g.12870646_12870647del GRCh37
NC_000012.10:g.12761913_12761914del NCBI36
NG_016341.1:g.5345_5346del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-128_-127del (CDKN1B) ENSP00000507272.1:n.-128_-127del
ENST00000682620.1:n.1631-1113_1631-1112del (CDKN1B)
ENST00000684771.1:n.585-1113_585-1112del (CDKN1B)
ENST00000228872.9:c.-128_-127del (CDKN1B) MANE Select ENSP00000228872.4:n.-128_-127del
ENST00000228872.8:c.-128_-127del (CDKN1B) ENSP00000228872.4:n.-128_-127del
ENST00000477087.1:n.155-1113_155-1112del (CDKN1B)
NM_004064.4:c.-128_-127del (CDKN1B) NP_004055.1:n.-128_-127del
XM_011520623.3:c.-2204_-2203del (GPR19) XP_011518925.1:n.-2204_-2203del
XM_017019216.2:c.-2232_-2231del (GPR19) XP_016874705.1:n.-2232_-2231del
NM_004064.5:c.-128_-127del (CDKN1B) MANE Select NP_004055.1:n.-128_-127del