Canonical Allele Identifier: CA2617685248

Gene: CDKN1B GPR19

Linked Data

• gnomAD v4: 12-12717642-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717642_12717643insC , CM000674.2:g.12717642_12717643insC	GRCh38
NC_000012.11:g.12870576_12870577insC , CM000674.1:g.12870576_12870577insC	GRCh37
NC_000012.10:g.12761843_12761844insC	NCBI36
NG_016341.1:g.5275_5276insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-198_-197insC (CDKN1B)	ENSP00000507272.1:n.-198_-197insC
ENST00000682620.1:n.1631-1183_1631-1182insC (CDKN1B)
ENST00000684771.1:n.585-1183_585-1182insC (CDKN1B)
ENST00000228872.9:c.-198_-197insC (CDKN1B) MANE Select	ENSP00000228872.4:n.-198_-197insC
ENST00000228872.8:c.-198_-197insC (CDKN1B)	ENSP00000228872.4:n.-198_-197insC
ENST00000477087.1:n.155-1183_155-1182insC (CDKN1B)
NM_004064.4:c.-198_-197insC (CDKN1B)	NP_004055.1:n.-198_-197insC
XM_011520623.3:c.-2137_-2136insG (GPR19)	XP_011518925.1:n.-2137_-2136insG
XM_017019216.2:c.-2165_-2164insG (GPR19)	XP_016874705.1:n.-2165_-2164insG
NM_004064.5:c.-198_-197insC (CDKN1B) MANE Select	NP_004055.1:n.-198_-197insC