Canonical Allele Identifier: CA2792650686

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229983_72229984insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG , CM000673.2:g.72229983_72229984insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	GRCh38
NC_000011.9:g.71941027_71941028insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG , CM000673.1:g.71941027_71941028insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	GRCh37
NC_000011.8:g.71618675_71618676insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	NCBI36
NG_023253.1:g.10146_10147insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG
NG_023253.2:g.10146_10147insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG MANE Select	ENSP00000298229.2:p.Arg302Ter
ENST00000298229.6:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	ENSP00000298229.2:p.Arg302Ter
ENST00000538751.5:c.177_178insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	ENSP00000444619.1:p.Arg60Ter
ENST00000540329.5:c.87_88insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	ENSP00000440018.1:p.Arg30Ter
ENST00000541756.5:c.705_706insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	ENSP00000446360.2:p.Arg236Ter
NM_001567.3:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	NP_001558.3:p.Arg302Ter
XM_005273978.3:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_005274035.1:p.Arg324Ter
XM_005273979.3:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_005274036.1:p.Arg324Ter
XM_011544999.1:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_011543301.1:p.Arg302Ter
XM_011545000.1:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_011543302.1:p.Arg324Ter
XM_005273979.4:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_005274036.1:p.Arg324Ter
XM_011544999.2:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_011543301.1:p.Arg302Ter
XM_024448501.1:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_024304269.1:p.Arg324Ter
XM_024448502.1:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_024304270.1:p.Arg324Ter
XM_024448503.1:c.939_940insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_024304271.1:p.Arg314Ter
XM_024448504.1:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_024304272.1:p.Arg302Ter
XM_024448505.1:c.969_970insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG	XP_024304273.1:p.Arg324Ter
NM_001567.4:c.903_904insTGATGAGCGCCGCGGCTGTCAAGTGCGGCCTGGCTTCCGACGAGAACGCCGACGATCTCAAGGACCTCGACGAAGCACG MANE Select	NP_001558.3:p.Arg302Ter