Canonical Allele Identifier: CA2017047163

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717449_12717450delinsCT , CM000674.2:g.12717449_12717450delinsCT	GRCh38
NC_000012.11:g.12870383_12870384delinsCT , CM000674.1:g.12870383_12870384delinsCT	GRCh37
NC_000012.10:g.12761650_12761651delinsCT	NCBI36
NG_016341.1:g.5082_5083delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-391_-390delinsCT (CDKN1B)	ENSP00000507272.1:n.-391_-390delinsCT
ENST00000682620.1:n.1631-1376_1631-1375delinsCT (CDKN1B)
ENST00000684771.1:n.585-1376_585-1375delinsCT (CDKN1B)
ENST00000228872.9:c.-391_-390delinsCT (CDKN1B) MANE Select	ENSP00000228872.4:n.-391_-390delinsCT
ENST00000228872.8:c.-391_-390delinsCT (CDKN1B)	ENSP00000228872.4:n.-391_-390delinsCT
ENST00000477087.1:n.155-1376_155-1375delinsCT (CDKN1B)
NM_004064.4:c.-391_-390delinsCT (CDKN1B)	NP_004055.1:n.-391_-390delinsCT
XM_011520623.3:c.-1944_-1943delinsAG (GPR19)	XP_011518925.1:n.-1944_-1943delinsAG
XM_017019216.2:c.-1972_-1971delinsAG (GPR19)	XP_016874705.1:n.-1972_-1971delinsAG
NM_004064.5:c.-391_-390delinsCT (CDKN1B) MANE Select	NP_004055.1:n.-391_-390delinsCT