Canonical Allele Identifier: CA2017047249

Gene: CDKN1B GPR19

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717566_12717586delinsACCCTCTCCGCTTGCCTGGTC , CM000674.2:g.12717566_12717586delinsACCCTCTCCGCTTGCCTGGTC	GRCh38
NC_000012.11:g.12870500_12870520delinsACCCTCTCCGCTTGCCTGGTC , CM000674.1:g.12870500_12870520delinsACCCTCTCCGCTTGCCTGGTC	GRCh37
NC_000012.10:g.12761767_12761787delinsACCCTCTCCGCTTGCCTGGTC	NCBI36
NG_016341.1:g.5199_5219delinsACCCTCTCCGCTTGCCTGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-274_-254delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B)	ENSP00000507272.1:n.-274_-254delinsACCCTCTCCGCTTGCCTGGTC
ENST00000682620.1:n.1631-1259_1631-1239delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B)
ENST00000684771.1:n.585-1259_585-1239delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B)
ENST00000228872.9:c.-274_-254delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B) MANE Select	ENSP00000228872.4:n.-274_-254delinsACCCTCTCCGCTTGCCTGGTC
ENST00000228872.8:c.-274_-254delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B)	ENSP00000228872.4:n.-274_-254delinsACCCTCTCCGCTTGCCTGGTC
ENST00000477087.1:n.155-1259_155-1239delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B)
NM_004064.4:c.-274_-254delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B)	NP_004055.1:n.-274_-254delinsACCCTCTCCGCTTGCCTGGTC
XM_011520623.3:c.-2080_-2060delinsGACCAGGCAAGCGGAGAGGGT (GPR19)	XP_011518925.1:n.-2080_-2060delinsGACCAGGCAAGCGGAGAGGGT
XM_017019216.2:c.-2108_-2088delinsGACCAGGCAAGCGGAGAGGGT (GPR19)	XP_016874705.1:n.-2108_-2088delinsGACCAGGCAAGCGGAGAGGGT
NM_004064.5:c.-274_-254delinsACCCTCTCCGCTTGCCTGGTC (CDKN1B) MANE Select	NP_004055.1:n.-274_-254delinsACCCTCTCCGCTTGCCTGGTC