Canonical Allele Identifier: CA2617685291

Gene: CDKN1B GPR19

Linked Data

• gnomAD v4: 12-12717683-A-AGCTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717685_12717689dup , CM000674.2:g.12717685_12717689dup	GRCh38
NC_000012.11:g.12870619_12870623dup , CM000674.1:g.12870619_12870623dup	GRCh37
NC_000012.10:g.12761886_12761890dup	NCBI36
NG_016341.1:g.5318_5322dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-155_-151dup (CDKN1B)	ENSP00000507272.1:n.-155_-151dup
ENST00000682620.1:n.1631-1140_1631-1136dup (CDKN1B)
ENST00000684771.1:n.585-1140_585-1136dup (CDKN1B)
ENST00000228872.9:c.-155_-151dup (CDKN1B) MANE Select	ENSP00000228872.4:n.-155_-151dup
ENST00000228872.8:c.-155_-151dup (CDKN1B)	ENSP00000228872.4:n.-155_-151dup
ENST00000477087.1:n.155-1140_155-1136dup (CDKN1B)
NM_004064.4:c.-155_-151dup (CDKN1B)	NP_004055.1:n.-155_-151dup
XM_011520623.3:c.-2182_-2178dup (GPR19)	XP_011518925.1:n.-2182_-2178dup
XM_017019216.2:c.-2210_-2206dup (GPR19)	XP_016874705.1:n.-2210_-2206dup
NM_004064.5:c.-155_-151dup (CDKN1B) MANE Select	NP_004055.1:n.-155_-151dup