Canonical Allele Identifier: CA2017047172

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717454_12717455delinsCT , CM000674.2:g.12717454_12717455delinsCT	GRCh38
NC_000012.11:g.12870388_12870389delinsCT , CM000674.1:g.12870388_12870389delinsCT	GRCh37
NC_000012.10:g.12761655_12761656delinsCT	NCBI36
NG_016341.1:g.5087_5088delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-386_-385delinsCT (CDKN1B)	ENSP00000507272.1:n.-386_-385delinsCT
ENST00000682620.1:n.1631-1371_1631-1370delinsCT (CDKN1B)
ENST00000684771.1:n.585-1371_585-1370delinsCT (CDKN1B)
ENST00000228872.9:c.-386_-385delinsCT (CDKN1B) MANE Select	ENSP00000228872.4:n.-386_-385delinsCT
ENST00000228872.8:c.-386_-385delinsCT (CDKN1B)	ENSP00000228872.4:n.-386_-385delinsCT
ENST00000477087.1:n.155-1371_155-1370delinsCT (CDKN1B)
NM_004064.4:c.-386_-385delinsCT (CDKN1B)	NP_004055.1:n.-386_-385delinsCT
XM_011520623.3:c.-1949_-1948delinsAG (GPR19)	XP_011518925.1:n.-1949_-1948delinsAG
XM_017019216.2:c.-1977_-1976delinsAG (GPR19)	XP_016874705.1:n.-1977_-1976delinsAG
NM_004064.5:c.-386_-385delinsCT (CDKN1B) MANE Select	NP_004055.1:n.-386_-385delinsCT