Canonical Allele Identifier: CA2689597039

Gene: CDKN2A

Linked Data

• gnomAD v4: 9-21968191-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968193del , CM000671.2:g.21968193del	GRCh38
NC_000009.11:g.21968192del , CM000671.1:g.21968192del	GRCh37
NC_000009.10:g.21958192del	NCBI36
NG_007485.1:g.31300del , LRG_11:g.31300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.*37del MANE Select	ENSP00000307101.5:n.*37del
ENST00000404796.3:c.348-61240del	ENSP00000385916.2:n.348-61240del
ENST00000579755.2:c.*152del MANE Plus Clinical	ENSP00000462950.1:n.*152del
ENST00000304494.9:c.*37del	ENSP00000307101.5:n.*37del
ENST00000361570.4:c.*37del	ENSP00000355153.4:n.*37del
ENST00000380151.3:c.782del	ENSP00000369496.3:n.782del
ENST00000404796.2:c.348-61240del	ENSP00000385916.2:n.348-61240del
ENST00000494262.5:c.*37del	ENSP00000464952.1:n.*37del
ENST00000498124.1:c.*201del	ENSP00000418915.1:n.*201del
ENST00000498628.6:c.*37del	ENSP00000467857.1:n.*37del
ENST00000530628.2:c.*78del	ENSP00000432664.2:n.*78del
ENST00000578845.2:c.*37del	ENSP00000467390.1:n.*37del
ENST00000579122.1:c.*17del	ENSP00000464202.1:n.*17del
ENST00000579755.1:c.*152del	ENSP00000462950.1:n.*152del
NM_000077.4:c.*37del , LRG_11t1:c.*37del	NP_000068.1:n.*37del
NM_001195132.1:c.*201del	NP_001182061.1:n.*201del
NM_058195.3:c.*152del , LRG_11t2:c.*152del	NP_478102.2:n.*152del
NM_058197.4:c.782del	NP_478104.2:n.782del
XM_005251343.1:c.*37del	XP_005251400.1:n.*37del
XM_011517679.1:c.*37del	XP_011515981.1:n.*37del
NM_001363763.1:c.*37del	NP_001350692.1:n.*37del
NM_001363763.2:c.*37del	NP_001350692.1:n.*37del
NM_000077.5:c.*37del MANE Select	NP_000068.1:n.*37del
NM_001195132.2:c.*201del	NP_001182061.1:n.*201del
NM_058195.4:c.*152del MANE Plus Clinical	NP_478102.2:n.*152del
NM_058197.5:c.*431del	NP_478104.2:n.*431del