Canonical Allele Identifier: CA1981898158

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230618_72230619delinsCG , CM000673.2:g.72230618_72230619delinsCG	GRCh38
NC_000011.9:g.71941662_71941663delinsCG , CM000673.1:g.71941662_71941663delinsCG	GRCh37
NC_000011.8:g.71619310_71619311delinsCG	NCBI36
NG_023253.1:g.10781_10782delinsCG
NG_023253.2:g.10781_10782delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.1197+150_1197+151delinsCG MANE Select	ENSP00000298229.2:n.1197+150_1197+151delinsCG
ENST00000298229.6:c.1197+150_1197+151delinsCG	ENSP00000298229.2:n.1197+150_1197+151delinsCG
ENST00000538751.5:c.471+150_471+151delinsCG	ENSP00000444619.1:n.471+150_471+151delinsCG
ENST00000541756.5:c.999+150_999+151delinsCG	ENSP00000446360.2:n.999+150_999+151delinsCG
NM_001567.3:c.1197+150_1197+151delinsCG	NP_001558.3:n.1197+150_1197+151delinsCG
XM_005273978.3:c.1263+150_1263+151delinsCG	XP_005274035.1:n.1263+150_1263+151delinsCG
XM_005273979.3:c.1263+150_1263+151delinsCG	XP_005274036.1:n.1263+150_1263+151delinsCG
XM_011544999.1:c.1197+150_1197+151delinsCG	XP_011543301.1:n.1197+150_1197+151delinsCG
XM_011545000.1:c.1263+150_1263+151delinsCG	XP_011543302.1:n.1263+150_1263+151delinsCG
XM_005273979.4:c.1263+150_1263+151delinsCG	XP_005274036.1:n.1263+150_1263+151delinsCG
XM_011544999.2:c.1197+150_1197+151delinsCG	XP_011543301.1:n.1197+150_1197+151delinsCG
XM_024448501.1:c.1263+150_1263+151delinsCG	XP_024304269.1:n.1263+150_1263+151delinsCG
XM_024448502.1:c.1263+150_1263+151delinsCG	XP_024304270.1:n.1263+150_1263+151delinsCG
XM_024448503.1:c.1233+150_1233+151delinsCG	XP_024304271.1:n.1233+150_1233+151delinsCG
XM_024448504.1:c.1197+150_1197+151delinsCG	XP_024304272.1:n.1197+150_1197+151delinsCG
XM_024448505.1:c.1263+150_1263+151delinsCG	XP_024304273.1:n.1263+150_1263+151delinsCG
NM_001567.4:c.1197+150_1197+151delinsCG MANE Select	NP_001558.3:n.1197+150_1197+151delinsCG