Canonical Allele Identifier: CA2617685215

Gene: CDKN1B GPR19

Linked Data

• gnomAD v4: 12-12717604-TCCCGCTCG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717607_12717614del , CM000674.2:g.12717607_12717614del	GRCh38
NC_000012.11:g.12870541_12870548del , CM000674.1:g.12870541_12870548del	GRCh37
NC_000012.10:g.12761808_12761815del	NCBI36
NG_016341.1:g.5240_5247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-233_-226del (CDKN1B)	ENSP00000507272.1:n.-233_-226del
ENST00000682620.1:n.1631-1218_1631-1211del (CDKN1B)
ENST00000684771.1:n.585-1218_585-1211del (CDKN1B)
ENST00000228872.9:c.-233_-226del (CDKN1B) MANE Select	ENSP00000228872.4:n.-233_-226del
ENST00000228872.8:c.-233_-226del (CDKN1B)	ENSP00000228872.4:n.-233_-226del
ENST00000477087.1:n.155-1218_155-1211del (CDKN1B)
NM_004064.4:c.-233_-226del (CDKN1B)	NP_004055.1:n.-233_-226del
XM_011520623.3:c.-2106_-2099del (GPR19)	XP_011518925.1:n.-2106_-2099del
XM_017019216.2:c.-2134_-2127del (GPR19)	XP_016874705.1:n.-2134_-2127del
NM_004064.5:c.-233_-226del (CDKN1B) MANE Select	NP_004055.1:n.-233_-226del