Canonical Allele Identifier: CA190727786

Gene: CDKN2A

Linked Data

• dbSNP Id: rs983922540
• gnomAD v3: 9-21968077-G-A
• gnomAD v4: 9-21968077-G-A
• MyVariant Identifiers: chr9:g.21968076G>A (hg19) ; chr9:g.21968077G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21968077G>A , CM000671.2:g.21968077G>A	GRCh38
NC_000009.11:g.21968076G>A , CM000671.1:g.21968076G>A	GRCh37
NC_000009.10:g.21958076G>A	NCBI36
NG_007485.1:g.31415C>T , LRG_11:g.31415C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.*152C>T MANE Select	ENSP00000307101.5:n.*152C>T
ENST00000404796.3:c.348-61356G>A	ENSP00000385916.2:n.348-61356G>A
ENST00000579755.2:c.*267C>T MANE Plus Clinical	ENSP00000462950.1:n.*267C>T
ENST00000304494.9:c.*152C>T	ENSP00000307101.5:n.*152C>T
ENST00000361570.4:c.*152C>T	ENSP00000355153.4:n.*152C>T
ENST00000404796.2:c.348-61356G>A	ENSP00000385916.2:n.348-61356G>A
ENST00000498124.1:c.*316C>T	ENSP00000418915.1:n.*316C>T
ENST00000530628.2:c.*193C>T	ENSP00000432664.2:n.*193C>T
ENST00000578845.2:c.*152C>T	ENSP00000467390.1:n.*152C>T
ENST00000579122.1:c.*132C>T	ENSP00000464202.1:n.*132C>T
ENST00000579755.1:c.*267C>T	ENSP00000462950.1:n.*267C>T
NM_000077.4:c.*152C>T , LRG_11t1:c.*152C>T	NP_000068.1:n.*152C>T
NM_001195132.1:c.*316C>T	NP_001182061.1:n.*316C>T
NM_058195.3:c.*267C>T , LRG_11t2:c.*267C>T	NP_478102.2:n.*267C>T
NM_058197.4:c.897C>T	NP_478104.2:n.897C>T
XM_005251343.1:c.*152C>T	XP_005251400.1:n.*152C>T
XM_011517679.1:c.*152C>T	XP_011515981.1:n.*152C>T
NM_001363763.1:c.*152C>T	NP_001350692.1:n.*152C>T
NM_001363763.2:c.*152C>T	NP_001350692.1:n.*152C>T
NM_000077.5:c.*152C>T MANE Select	NP_000068.1:n.*152C>T
NM_001195132.2:c.*316C>T	NP_001182061.1:n.*316C>T
NM_058195.4:c.*267C>T MANE Plus Clinical	NP_478102.2:n.*267C>T
NM_058197.5:c.*546C>T	NP_478104.2:n.*546C>T