Canonical Allele Identifier: CA373085066

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1162344499
• MyVariant Identifiers: chr9:g.21968235G>A (hg19) ; chr9:g.21968236G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968236G>A , CM000671.2:g.21968236G>A	GRCh38
NC_000009.11:g.21968235G>A , CM000671.1:g.21968235G>A	GRCh37
NC_000009.10:g.21958235G>A	NCBI36
NG_007485.1:g.31256C>T , LRG_11:g.31256C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.464C>T MANE Select	ENSP00000307101.5:p.Pro155Leu
ENST00000404796.3:c.348-61197G>A	ENSP00000385916.2:n.348-61197G>A
ENST00000579755.2:c.*108C>T MANE Plus Clinical	ENSP00000462950.1:n.*108C>T
ENST00000304494.9:c.464C>T	ENSP00000307101.5:p.Pro155Leu
ENST00000361570.4:c.506C>T	ENSP00000355153.4:p.Pro169Leu
ENST00000380151.3:c.738C>T	ENSP00000369496.3:n.738C>T
ENST00000404796.2:c.348-61197G>A	ENSP00000385916.2:n.348-61197G>A
ENST00000494262.5:c.311C>T	ENSP00000464952.1:p.Pro104Leu
ENST00000498124.1:c.*157C>T	ENSP00000418915.1:n.*157C>T
ENST00000498628.6:c.311C>T	ENSP00000467857.1:p.Pro104Leu
ENST00000530628.2:c.*34C>T	ENSP00000432664.2:n.*34C>T
ENST00000578845.2:c.311C>T	ENSP00000467390.1:p.Pro104Leu
ENST00000579122.1:c.390C>T	ENSP00000464202.1:p.Pro130=
ENST00000579755.1:c.*108C>T	ENSP00000462950.1:n.*108C>T
NM_000077.4:c.464C>T , LRG_11t1:c.464C>T	NP_000068.1:p.Pro155Leu
NM_001195132.1:c.*157C>T	NP_001182061.1:n.*157C>T
NM_058195.3:c.*108C>T , LRG_11t2:c.*108C>T	NP_478102.2:n.*108C>T
NM_058197.4:c.738C>T	NP_478104.2:n.738C>T
XM_005251343.1:c.311C>T	XP_005251400.1:p.Pro104Leu
XM_011517679.1:c.311C>T	XP_011515981.1:p.Pro104Leu
NM_001363763.1:c.311C>T	NP_001350692.1:p.Pro104Leu
NM_001363763.2:c.311C>T	NP_001350692.1:p.Pro104Leu
NM_000077.5:c.464C>T MANE Select	NP_000068.1:p.Pro155Leu
NM_001195132.2:c.*157C>T	NP_001182061.1:n.*157C>T
NM_058195.4:c.*108C>T MANE Plus Clinical	NP_478102.2:n.*108C>T
NM_058197.5:c.*387C>T	NP_478104.2:n.*387C>T