Canonical Allele Identifier: CA2017047173
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

dbSNP Id: rs1946476258

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717455del , CM000674.2:g.12717455del GRCh38
NC_000012.11:g.12870389del , CM000674.1:g.12870389del GRCh37
NC_000012.10:g.12761656del NCBI36
NG_016341.1:g.5088del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-385del (CDKN1B) ENSP00000507272.1:n.-385del
ENST00000682620.1:n.1631-1370del (CDKN1B)
ENST00000684771.1:n.585-1370del (CDKN1B)
ENST00000228872.9:c.-385del (CDKN1B) MANE Select ENSP00000228872.4:n.-385del
ENST00000228872.8:c.-385del (CDKN1B) ENSP00000228872.4:n.-385del
ENST00000477087.1:n.155-1370del (CDKN1B)
NM_004064.4:c.-385del (CDKN1B) NP_004055.1:n.-385del
XM_011520623.3:c.-1949del (GPR19) XP_011518925.1:n.-1949del
XM_017019216.2:c.-1977del (GPR19) XP_016874705.1:n.-1977del
NM_004064.5:c.-385del (CDKN1B) MANE Select NP_004055.1:n.-385del