Canonical Allele Identifier: CA1839172496

Gene: CDKN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21974601_21974602delinsGA , CM000671.2:g.21974601_21974602delinsGA	GRCh38
NC_000009.11:g.21974600_21974601delinsGA , CM000671.1:g.21974600_21974601delinsGA	GRCh37
NC_000009.10:g.21964600_21964601delinsGA	NCBI36
NG_007485.1:g.24890_24891delinsTC , LRG_11:g.24890_24891delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304494.10:c.150+76_150+77delinsTC MANE Select	ENSP00000307101.5:n.150+76_150+77delinsTC
ENST00000404796.3:c.348-54832_348-54831delinsGA	ENSP00000385916.2:n.348-54832_348-54831delinsGA
ENST00000579755.2:c.194-3394_194-3393delinsTC MANE Plus Clinical	ENSP00000462950.1:n.194-3394_194-3393delinsTC
ENST00000304494.9:c.150+76_150+77delinsTC	ENSP00000307101.5:n.150+76_150+77delinsTC
ENST00000361570.4:c.194-3394_194-3393delinsTC	ENSP00000355153.4:n.194-3394_194-3393delinsTC
ENST00000380151.3:c.226_227delinsTC	ENSP00000369496.3:p.Ser76=
ENST00000404796.2:c.348-54832_348-54831delinsGA	ENSP00000385916.2:n.348-54832_348-54831delinsGA
ENST00000494262.5:c.-3-3394_-3-3393delinsTC	ENSP00000464952.1:n.-3-3394_-3-3393delinsTC
ENST00000498124.1:c.150+76_150+77delinsTC	ENSP00000418915.1:n.150+76_150+77delinsTC
ENST00000498628.6:c.-3-3394_-3-3393delinsTC	ENSP00000467857.1:n.-3-3394_-3-3393delinsTC
ENST00000530628.2:c.194-3394_194-3393delinsTC	ENSP00000432664.2:n.194-3394_194-3393delinsTC
ENST00000579122.1:c.150+76_150+77delinsTC	ENSP00000464202.1:n.150+76_150+77delinsTC
ENST00000579755.1:c.194-3394_194-3393delinsTC	ENSP00000462950.1:n.194-3394_194-3393delinsTC
NM_000077.4:c.150+76_150+77delinsTC , LRG_11t1:c.150+76_150+77delinsTC	NP_000068.1:n.150+76_150+77delinsTC
NM_001195132.1:c.150+76_150+77delinsTC	NP_001182061.1:n.150+76_150+77delinsTC
NM_058195.3:c.194-3394_194-3393delinsTC , LRG_11t2:c.194-3394_194-3393delinsTC	NP_478102.2:n.194-3394_194-3393delinsTC
NM_058197.4:c.226_227delinsTC	NP_478104.2:p.Ser76=
XM_011517675.1:c.150+76_150+77delinsTC	XP_011515977.1:n.150+76_150+77delinsTC
XM_011517676.1:c.150+76_150+77delinsTC	XP_011515978.1:n.150+76_150+77delinsTC
XM_011517679.1:c.-3-3394_-3-3393delinsTC	XP_011515981.1:n.-3-3394_-3-3393delinsTC
XR_929159.1:n.551+76_551+77delinsTC
XR_929161.1:n.341-3394_341-3393delinsTC
XR_929162.1:n.341-3394_341-3393delinsTC
XR_929163.1:n.290-3394_290-3393delinsTC
NM_001363763.1:c.-3-3394_-3-3393delinsTC	NP_001350692.1:n.-3-3394_-3-3393delinsTC
XM_011517675.2:c.150+76_150+77delinsTC	XP_011515977.1:n.150+76_150+77delinsTC
XM_011517676.2:c.150+76_150+77delinsTC	XP_011515978.1:n.150+76_150+77delinsTC
XR_929159.2:n.480+76_480+77delinsTC
NM_001363763.2:c.-3-3394_-3-3393delinsTC	NP_001350692.1:n.-3-3394_-3-3393delinsTC
NM_000077.5:c.150+76_150+77delinsTC MANE Select	NP_000068.1:n.150+76_150+77delinsTC
NM_001195132.2:c.150+76_150+77delinsTC	NP_001182061.1:n.150+76_150+77delinsTC
NM_058195.4:c.194-3394_194-3393delinsTC MANE Plus Clinical	NP_478102.2:n.194-3394_194-3393delinsTC
NM_058197.5:c.226_227delinsTC	NP_478104.2:p.Ser76=