Canonical Allele Identifier: CA1839178824

Gene: CDKN2A

Linked Data

• dbSNP Id: rs1820360219

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21988854C>G , CM000671.2:g.21988854C>G	GRCh38
NC_000009.11:g.21988853C>G , CM000671.1:g.21988853C>G	GRCh37
NC_000009.10:g.21978853C>G	NCBI36
NG_007485.1:g.10638G>C , LRG_11:g.10638G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-40579C>G	ENSP00000385916.2:n.348-40579C>G
ENST00000579755.2:c.193+5285G>C MANE Plus Clinical	ENSP00000462950.1:n.193+5285G>C
ENST00000361570.4:c.193+5285G>C	ENSP00000355153.4:n.193+5285G>C
ENST00000404796.2:c.348-40579C>G	ENSP00000385916.2:n.348-40579C>G
ENST00000494262.5:c.-4+5028G>C	ENSP00000464952.1:n.-4+5028G>C
ENST00000498628.6:c.-4+5967G>C	ENSP00000467857.1:n.-4+5967G>C
ENST00000530628.2:c.193+5285G>C	ENSP00000432664.2:n.193+5285G>C
ENST00000579755.1:c.193+5285G>C	ENSP00000462950.1:n.193+5285G>C
NM_058195.3:c.193+5285G>C , LRG_11t2:c.193+5285G>C	NP_478102.2:n.193+5285G>C
XM_011517678.1:c.*1076G>C	XP_011515980.1:n.*1076G>C
XM_011517679.1:c.-4+5967G>C	XP_011515981.1:n.-4+5967G>C
XR_929161.1:n.340+5285G>C
XR_929162.1:n.340+5285G>C
XR_929163.1:n.289+5285G>C
NM_001363763.1:c.-4+5967G>C	NP_001350692.1:n.-4+5967G>C
NM_001363763.2:c.-4+5967G>C	NP_001350692.1:n.-4+5967G>C
NM_058195.4:c.193+5285G>C MANE Plus Clinical	NP_478102.2:n.193+5285G>C