Canonical Allele Identifier: CA2017047108

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717383_12717387delinsCCCTT , CM000674.2:g.12717383_12717387delinsCCCTT	GRCh38
NC_000012.11:g.12870317_12870321delinsCCCTT , CM000674.1:g.12870317_12870321delinsCCCTT	GRCh37
NC_000012.10:g.12761584_12761588delinsCCCTT	NCBI36
NG_016341.1:g.5016_5020delinsCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-457_-453delinsCCCTT (CDKN1B)	ENSP00000507272.1:n.-457_-453delinsCCCTT
ENST00000682620.1:n.1631-1442_1631-1438delinsCCCTT (CDKN1B)
ENST00000684771.1:n.585-1442_585-1438delinsCCCTT (CDKN1B)
ENST00000228872.9:c.-457_-453delinsCCCTT (CDKN1B) MANE Select	ENSP00000228872.4:n.-457_-453delinsCCCTT
ENST00000228872.8:c.-457_-453delinsCCCTT (CDKN1B)	ENSP00000228872.4:n.-457_-453delinsCCCTT
ENST00000477087.1:n.155-1442_155-1438delinsCCCTT (CDKN1B)
NM_004064.4:c.-457_-453delinsCCCTT (CDKN1B)	NP_004055.1:n.-457_-453delinsCCCTT
XM_011520623.3:c.-1881_-1877delinsAAGGG (GPR19)	XP_011518925.1:n.-1881_-1877delinsAAGGG
XM_017019216.2:c.-1909_-1905delinsAAGGG (GPR19)	XP_016874705.1:n.-1909_-1905delinsAAGGG
NM_004064.5:c.-457_-453delinsCCCTT (CDKN1B) MANE Select	NP_004055.1:n.-457_-453delinsCCCTT