Canonical Allele Identifier: CA373085069

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1060501271
• MyVariant Identifiers: chr9:g.21968236G>T (hg19) ; chr9:g.21968237G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968237G>T , CM000671.2:g.21968237G>T	GRCh38
NC_000009.11:g.21968236G>T , CM000671.1:g.21968236G>T	GRCh37
NC_000009.10:g.21958236G>T	NCBI36
NG_007485.1:g.31255C>A , LRG_11:g.31255C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.463C>A MANE Select	ENSP00000307101.5:p.Pro155Thr
ENST00000404796.3:c.348-61196G>T	ENSP00000385916.2:n.348-61196G>T
ENST00000579755.2:c.*107C>A MANE Plus Clinical	ENSP00000462950.1:n.*107C>A
ENST00000304494.9:c.463C>A	ENSP00000307101.5:p.Pro155Thr
ENST00000361570.4:c.505C>A	ENSP00000355153.4:p.Pro169Thr
ENST00000380151.3:c.737C>A	ENSP00000369496.3:n.737C>A
ENST00000404796.2:c.348-61196G>T	ENSP00000385916.2:n.348-61196G>T
ENST00000494262.5:c.310C>A	ENSP00000464952.1:p.Pro104Thr
ENST00000498124.1:c.*156C>A	ENSP00000418915.1:n.*156C>A
ENST00000498628.6:c.310C>A	ENSP00000467857.1:p.Pro104Thr
ENST00000530628.2:c.*33C>A	ENSP00000432664.2:n.*33C>A
ENST00000578845.2:c.310C>A	ENSP00000467390.1:p.Pro104Thr
ENST00000579122.1:c.389C>A	ENSP00000464202.1:p.Pro130His
ENST00000579755.1:c.*107C>A	ENSP00000462950.1:n.*107C>A
NM_000077.4:c.463C>A , LRG_11t1:c.463C>A	NP_000068.1:p.Pro155Thr
NM_001195132.1:c.*156C>A	NP_001182061.1:n.*156C>A
NM_058195.3:c.*107C>A , LRG_11t2:c.*107C>A	NP_478102.2:n.*107C>A
NM_058197.4:c.737C>A	NP_478104.2:n.737C>A
XM_005251343.1:c.310C>A	XP_005251400.1:p.Pro104Thr
XM_011517679.1:c.310C>A	XP_011515981.1:p.Pro104Thr
NM_001363763.1:c.310C>A	NP_001350692.1:p.Pro104Thr
NM_001363763.2:c.310C>A	NP_001350692.1:p.Pro104Thr
NM_000077.5:c.463C>A MANE Select	NP_000068.1:p.Pro155Thr
NM_001195132.2:c.*156C>A	NP_001182061.1:n.*156C>A
NM_058195.4:c.*107C>A MANE Plus Clinical	NP_478102.2:n.*107C>A
NM_058197.5:c.*386C>A	NP_478104.2:n.*386C>A