Canonical Allele Identifier: CA919026429

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs1592280315
• gnomAD v4: 12-12717450-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717453_12717454del , CM000674.2:g.12717453_12717454del	GRCh38
NC_000012.11:g.12870387_12870388del , CM000674.1:g.12870387_12870388del	GRCh37
NC_000012.10:g.12761654_12761655del	NCBI36
NG_016341.1:g.5086_5087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-387_-386del (CDKN1B)	ENSP00000507272.1:n.-387_-386del
ENST00000682620.1:n.1631-1372_1631-1371del (CDKN1B)
ENST00000684771.1:n.585-1372_585-1371del (CDKN1B)
ENST00000228872.9:c.-387_-386del (CDKN1B) MANE Select	ENSP00000228872.4:n.-387_-386del
ENST00000228872.8:c.-387_-386del (CDKN1B)	ENSP00000228872.4:n.-387_-386del
ENST00000477087.1:n.155-1372_155-1371del (CDKN1B)
NM_004064.4:c.-387_-386del (CDKN1B)	NP_004055.1:n.-387_-386del
XM_011520623.3:c.-1946_-1945del (GPR19)	XP_011518925.1:n.-1946_-1945del
XM_017019216.2:c.-1974_-1973del (GPR19)	XP_016874705.1:n.-1974_-1973del
NM_004064.5:c.-387_-386del (CDKN1B) MANE Select	NP_004055.1:n.-387_-386del