Canonical Allele Identifier: CA1981895586

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225320_72225323delinsTGAG , CM000673.2:g.72225320_72225323delinsTGAG	GRCh38
NC_000011.9:g.71936364_71936367delinsTGAG , CM000673.1:g.71936364_71936367delinsTGAG	GRCh37
NC_000011.8:g.71614012_71614015delinsTGAG	NCBI36
NG_023253.1:g.5483_5486delinsTGAG
NG_023253.2:g.5483_5486delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+154_182+157delinsTGAG MANE Select	ENSP00000298229.2:n.182+154_182+157delinsTGAG
ENST00000298229.6:c.182+154_182+157delinsTGAG	ENSP00000298229.2:n.182+154_182+157delinsTGAG
ENST00000541544.1:n.98+154_98+157delinsTGAG
NM_001567.3:c.182+154_182+157delinsTGAG	NP_001558.3:n.182+154_182+157delinsTGAG
XM_005273978.3:c.182+154_182+157delinsTGAG	XP_005274035.1:n.182+154_182+157delinsTGAG
XM_005273979.3:c.182+154_182+157delinsTGAG	XP_005274036.1:n.182+154_182+157delinsTGAG
XM_011544999.1:c.182+154_182+157delinsTGAG	XP_011543301.1:n.182+154_182+157delinsTGAG
XM_011545000.1:c.182+154_182+157delinsTGAG	XP_011543302.1:n.182+154_182+157delinsTGAG
XM_005273979.4:c.182+154_182+157delinsTGAG	XP_005274036.1:n.182+154_182+157delinsTGAG
XM_011544999.2:c.182+154_182+157delinsTGAG	XP_011543301.1:n.182+154_182+157delinsTGAG
XM_024448501.1:c.182+154_182+157delinsTGAG	XP_024304269.1:n.182+154_182+157delinsTGAG
XM_024448502.1:c.182+154_182+157delinsTGAG	XP_024304270.1:n.182+154_182+157delinsTGAG
XM_024448503.1:c.62-130_62-127delinsTGAG	XP_024304271.1:n.62-130_62-127delinsTGAG
XM_024448504.1:c.182+154_182+157delinsTGAG	XP_024304272.1:n.182+154_182+157delinsTGAG
XM_024448505.1:c.182+154_182+157delinsTGAG	XP_024304273.1:n.182+154_182+157delinsTGAG
NM_001567.4:c.182+154_182+157delinsTGAG MANE Select	NP_001558.3:n.182+154_182+157delinsTGAG