Canonical Allele Identifier: CA1839172820

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974695_21974696delinsCG , CM000671.2:g.21974695_21974696delinsCG	GRCh38
NC_000009.11:g.21974694_21974695delinsCG , CM000671.1:g.21974694_21974695delinsCG	GRCh37
NC_000009.10:g.21964694_21964695delinsCG	NCBI36
NG_007485.1:g.24796_24797delinsCG , LRG_11:g.24796_24797delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.132_133delinsCG MANE Select	ENSP00000307101.5:p.Tyr44=
ENST00000404796.3:c.348-54738_348-54737delinsCG	ENSP00000385916.2:n.348-54738_348-54737delinsCG
ENST00000579755.2:c.194-3488_194-3487delinsCG MANE Plus Clinical	ENSP00000462950.1:n.194-3488_194-3487delinsCG
ENST00000304494.9:c.132_133delinsCG	ENSP00000307101.5:p.Tyr44=
ENST00000361570.4:c.194-3488_194-3487delinsCG	ENSP00000355153.4:n.194-3488_194-3487delinsCG
ENST00000380151.3:c.132_133delinsCG	ENSP00000369496.3:p.Tyr44=
ENST00000404796.2:c.348-54738_348-54737delinsCG	ENSP00000385916.2:n.348-54738_348-54737delinsCG
ENST00000494262.5:c.-3-3488_-3-3487delinsCG	ENSP00000464952.1:n.-3-3488_-3-3487delinsCG
ENST00000498124.1:c.132_133delinsCG	ENSP00000418915.1:p.Tyr44=
ENST00000498628.6:c.-3-3488_-3-3487delinsCG	ENSP00000467857.1:n.-3-3488_-3-3487delinsCG
ENST00000530628.2:c.194-3488_194-3487delinsCG	ENSP00000432664.2:n.194-3488_194-3487delinsCG
ENST00000579122.1:c.132_133delinsCG	ENSP00000464202.1:p.Tyr44=
ENST00000579755.1:c.194-3488_194-3487delinsCG	ENSP00000462950.1:n.194-3488_194-3487delinsCG
NM_000077.4:c.132_133delinsCG , LRG_11t1:c.132_133delinsCG	NP_000068.1:p.Tyr44=
NM_001195132.1:c.132_133delinsCG	NP_001182061.1:p.Tyr44=
NM_058195.3:c.194-3488_194-3487delinsCG , LRG_11t2:c.194-3488_194-3487delinsCG	NP_478102.2:n.194-3488_194-3487delinsCG
NM_058197.4:c.132_133delinsCG	NP_478104.2:p.Tyr44=
XM_011517675.1:c.132_133delinsCG	XP_011515977.1:p.Tyr44=
XM_011517676.1:c.132_133delinsCG	XP_011515978.1:p.Tyr44=
XM_011517679.1:c.-3-3488_-3-3487delinsCG	XP_011515981.1:n.-3-3488_-3-3487delinsCG
XR_929159.1:n.533_534delinsCG
XR_929161.1:n.341-3488_341-3487delinsCG
XR_929162.1:n.341-3488_341-3487delinsCG
XR_929163.1:n.290-3488_290-3487delinsCG
NM_001363763.1:c.-3-3488_-3-3487delinsCG	NP_001350692.1:n.-3-3488_-3-3487delinsCG
XM_011517675.2:c.132_133delinsCG	XP_011515977.1:p.Tyr44=
XM_011517676.2:c.132_133delinsCG	XP_011515978.1:p.Tyr44=
XR_929159.2:n.462_463delinsCG
NM_001363763.2:c.-3-3488_-3-3487delinsCG	NP_001350692.1:n.-3-3488_-3-3487delinsCG
NM_000077.5:c.132_133delinsCG MANE Select	NP_000068.1:p.Tyr44=
NM_001195132.2:c.132_133delinsCG	NP_001182061.1:p.Tyr44=
NM_058195.4:c.194-3488_194-3487delinsCG MANE Plus Clinical	NP_478102.2:n.194-3488_194-3487delinsCG
NM_058197.5:c.132_133delinsCG	NP_478104.2:p.Tyr44=