Canonical Allele Identifier: CA2499219821

Gene: CDKN2A

Linked Data

• ClinVar Variation Id: 1132894
• ClinVar RCV Id: RCV001467306
• dbSNP Id: rs1473161353

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968230C>T , CM000671.2:g.21968230C>T	GRCh38
NC_000009.11:g.21968229C>T , CM000671.1:g.21968229C>T	GRCh37
NC_000009.10:g.21958229C>T	NCBI36
NG_007485.1:g.31262G>A , LRG_11:g.31262G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.470G>A MANE Select	ENSP00000307101.5:p.Ter157=
ENST00000404796.3:c.348-61203C>T	ENSP00000385916.2:n.348-61203C>T
ENST00000579755.2:c.*114G>A MANE Plus Clinical	ENSP00000462950.1:n.*114G>A
ENST00000304494.9:c.470G>A	ENSP00000307101.5:p.Ter157=
ENST00000361570.4:c.512G>A	ENSP00000355153.4:p.Ter171=
ENST00000380151.3:c.744G>A	ENSP00000369496.3:n.744G>A
ENST00000404796.2:c.348-61203C>T	ENSP00000385916.2:n.348-61203C>T
ENST00000494262.5:c.317G>A	ENSP00000464952.1:p.Ter106=
ENST00000498124.1:c.*163G>A	ENSP00000418915.1:n.*163G>A
ENST00000498628.6:c.317G>A	ENSP00000467857.1:p.Ter106=
ENST00000530628.2:c.*40G>A	ENSP00000432664.2:n.*40G>A
ENST00000578845.2:c.317G>A	ENSP00000467390.1:p.Ter106=
ENST00000579122.1:c.396G>A	ENSP00000464202.1:p.Leu132=
ENST00000579755.1:c.*114G>A	ENSP00000462950.1:n.*114G>A
NM_000077.4:c.470G>A , LRG_11t1:c.470G>A	NP_000068.1:p.Ter157=
NM_001195132.1:c.*163G>A	NP_001182061.1:n.*163G>A
NM_058195.3:c.*114G>A , LRG_11t2:c.*114G>A	NP_478102.2:n.*114G>A
NM_058197.4:c.744G>A	NP_478104.2:n.744G>A
XM_005251343.1:c.317G>A	XP_005251400.1:p.Ter106=
XM_011517679.1:c.317G>A	XP_011515981.1:p.Ter106=
NM_001363763.1:c.317G>A	NP_001350692.1:p.Ter106=
NM_001363763.2:c.317G>A	NP_001350692.1:p.Ter106=
NM_000077.5:c.470G>A MANE Select	NP_000068.1:p.Ter157=
NM_001195132.2:c.*163G>A	NP_001182061.1:n.*163G>A
NM_058195.4:c.*114G>A MANE Plus Clinical	NP_478102.2:n.*114G>A
NM_058197.5:c.*393G>A	NP_478104.2:n.*393G>A