Canonical Allele Identifier: CA586896622

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1258900515
• gnomAD v2: 9-21971944-AAAAC-A
• gnomAD v3: 9-21971945-AAAAC-A
• gnomAD v4: 9-21971945-AAAAC-A
• MyVariant Identifiers: chr9:g.21971945_21971948del (hg19) ; chr9:g.21971946_21971949del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21971948_21971951del , CM000671.2:g.21971948_21971951del	GRCh38
NC_000009.11:g.21971947_21971950del , CM000671.1:g.21971947_21971950del	GRCh37
NC_000009.10:g.21961947_21961950del	NCBI36
NG_007485.1:g.27543_27546del , LRG_11:g.27543_27546del

Transcript Alleles

HGVS	Amino-acid change
ENST00000304494.10:c.151-741_151-738del MANE Select	ENSP00000307101.5:n.151-741_151-738del
ENST00000404796.3:c.348-57485_348-57482del	ENSP00000385916.2:n.348-57485_348-57482del
ENST00000579755.2:c.194-741_194-738del MANE Plus Clinical	ENSP00000462950.1:n.194-741_194-738del
ENST00000304494.9:c.151-741_151-738del	ENSP00000307101.5:n.151-741_151-738del
ENST00000361570.4:c.194-741_194-738del	ENSP00000355153.4:n.194-741_194-738del
ENST00000380151.3:c.425-741_425-738del	ENSP00000369496.3:n.425-741_425-738del
ENST00000404796.2:c.348-57485_348-57482del	ENSP00000385916.2:n.348-57485_348-57482del
ENST00000494262.5:c.-3-741_-3-738del	ENSP00000464952.1:n.-3-741_-3-738del
ENST00000498124.1:c.151-741_151-738del	ENSP00000418915.1:n.151-741_151-738del
ENST00000498628.6:c.-3-741_-3-738del	ENSP00000467857.1:n.-3-741_-3-738del
ENST00000530628.2:c.194-741_194-738del	ENSP00000432664.2:n.194-741_194-738del
ENST00000579122.1:c.151-741_151-738del	ENSP00000464202.1:n.151-741_151-738del
ENST00000579755.1:c.194-741_194-738del	ENSP00000462950.1:n.194-741_194-738del
NM_000077.4:c.151-741_151-738del , LRG_11t1:c.151-741_151-738del	NP_000068.1:n.151-741_151-738del
NM_001195132.1:c.151-741_151-738del	NP_001182061.1:n.151-741_151-738del
NM_058195.3:c.194-741_194-738del , LRG_11t2:c.194-741_194-738del	NP_478102.2:n.194-741_194-738del
NM_058197.4:c.425-741_425-738del	NP_478104.2:n.425-741_425-738del
XM_011517675.1:c.151-741_151-738del	XP_011515977.1:n.151-741_151-738del
XM_011517676.1:c.151-741_151-738del	XP_011515978.1:n.151-741_151-738del
XM_011517679.1:c.-3-741_-3-738del	XP_011515981.1:n.-3-741_-3-738del
XR_929159.1:n.552-741_552-738del
XR_929161.1:n.341-741_341-738del
XR_929162.1:n.341-741_341-738del
XR_929163.1:n.290-741_290-738del
NM_001363763.1:c.-3-741_-3-738del	NP_001350692.1:n.-3-741_-3-738del
XM_011517675.2:c.151-741_151-738del	XP_011515977.1:n.151-741_151-738del
XM_011517676.2:c.151-741_151-738del	XP_011515978.1:n.151-741_151-738del
XR_929159.2:n.481-741_481-738del
NM_001363763.2:c.-3-741_-3-738del	NP_001350692.1:n.-3-741_-3-738del
NM_000077.5:c.151-741_151-738del MANE Select	NP_000068.1:n.151-741_151-738del
NM_001195132.2:c.151-741_151-738del	NP_001182061.1:n.151-741_151-738del
NM_058195.4:c.194-741_194-738del MANE Plus Clinical	NP_478102.2:n.194-741_194-738del
NM_058197.5:c.*74-741_*74-738del	NP_478104.2:n.*74-741_*74-738del