Canonical Allele Identifier: CA1839173937

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21975026_21975027delinsAG , CM000671.2:g.21975026_21975027delinsAG	GRCh38
NC_000009.11:g.21975025_21975026delinsAG , CM000671.1:g.21975025_21975026delinsAG	GRCh37
NC_000009.10:g.21965025_21965026delinsAG	NCBI36
NG_007485.1:g.24465_24466delinsCT , LRG_11:g.24465_24466delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.348-54407_348-54406delinsAG	ENSP00000385916.2:n.348-54407_348-54406delinsAG
ENST00000579755.2:c.194-3819_194-3818delinsCT MANE Plus Clinical	ENSP00000462950.1:n.194-3819_194-3818delinsCT
ENST00000304494.9:c.-200_-199delinsCT	ENSP00000307101.5:n.-200_-199delinsCT
ENST00000361570.4:c.194-3819_194-3818delinsCT	ENSP00000355153.4:n.194-3819_194-3818delinsCT
ENST00000404796.2:c.348-54407_348-54406delinsAG	ENSP00000385916.2:n.348-54407_348-54406delinsAG
ENST00000494262.5:c.-3-3819_-3-3818delinsCT	ENSP00000464952.1:n.-3-3819_-3-3818delinsCT
ENST00000498628.6:c.-3-3819_-3-3818delinsCT	ENSP00000467857.1:n.-3-3819_-3-3818delinsCT
ENST00000530628.2:c.194-3819_194-3818delinsCT	ENSP00000432664.2:n.194-3819_194-3818delinsCT
ENST00000579755.1:c.194-3819_194-3818delinsCT	ENSP00000462950.1:n.194-3819_194-3818delinsCT
NM_000077.4:c.-200_-199delinsCT , LRG_11t1:c.-200_-199delinsCT	NP_000068.1:n.-200_-199delinsCT
NM_001195132.1:c.-200_-199delinsCT	NP_001182061.1:n.-200_-199delinsCT
NM_058195.3:c.194-3819_194-3818delinsCT , LRG_11t2:c.194-3819_194-3818delinsCT	NP_478102.2:n.194-3819_194-3818delinsCT
XM_011517675.1:c.-200_-199delinsCT	XP_011515977.1:n.-200_-199delinsCT
XM_011517676.1:c.-200_-199delinsCT	XP_011515978.1:n.-200_-199delinsCT
XM_011517679.1:c.-3-3819_-3-3818delinsCT	XP_011515981.1:n.-3-3819_-3-3818delinsCT
XR_929159.1:n.202_203delinsCT
XR_929161.1:n.341-3819_341-3818delinsCT
XR_929162.1:n.341-3819_341-3818delinsCT
XR_929163.1:n.290-3819_290-3818delinsCT
NM_001363763.1:c.-3-3819_-3-3818delinsCT	NP_001350692.1:n.-3-3819_-3-3818delinsCT
XM_011517675.2:c.-200_-199delinsCT	XP_011515977.1:n.-200_-199delinsCT
XM_011517676.2:c.-200_-199delinsCT	XP_011515978.1:n.-200_-199delinsCT
XR_929159.2:n.131_132delinsCT
NM_001363763.2:c.-3-3819_-3-3818delinsCT	NP_001350692.1:n.-3-3819_-3-3818delinsCT
NM_058195.4:c.194-3819_194-3818delinsCT MANE Plus Clinical	NP_478102.2:n.194-3819_194-3818delinsCT