Canonical Allele Identifier: CA1981895592

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225333_72225357delinsAGGGGCACTTCCTGCTGTGTGTCTG , CM000673.2:g.72225333_72225357delinsAGGGGCACTTCCTGCTGTGTGTCTG	GRCh38
NC_000011.9:g.71936377_71936401delinsAGGGGCACTTCCTGCTGTGTGTCTG , CM000673.1:g.71936377_71936401delinsAGGGGCACTTCCTGCTGTGTGTCTG	GRCh37
NC_000011.8:g.71614025_71614049delinsAGGGGCACTTCCTGCTGTGTGTCTG	NCBI36
NG_023253.1:g.5496_5520delinsAGGGGCACTTCCTGCTGTGTGTCTG
NG_023253.2:g.5496_5520delinsAGGGGCACTTCCTGCTGTGTGTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG MANE Select	ENSP00000298229.2:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGT...
ENST00000298229.6:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	ENSP00000298229.2:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGT...
ENST00000541544.1:n.98+167_98+191delinsAGGGGCACTTCCTGCTGTGTGTCTG
NM_001567.3:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	NP_001558.3:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG
XM_005273978.3:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_005274035.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_005273979.3:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_005274036.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_011544999.1:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_011543301.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_011545000.1:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_011543302.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_005273979.4:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_005274036.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_011544999.2:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_011543301.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_024448501.1:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_024304269.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_024448502.1:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_024304270.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_024448503.1:c.62-117_62-93delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_024304271.1:n.62-117_62-93delinsAGGGGCACTTCCTGCTGTGTGTCTG
XM_024448504.1:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_024304272.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
XM_024448505.1:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG	XP_024304273.1:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTC...
NM_001567.4:c.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG MANE Select	NP_001558.3:n.182+167_182+191delinsAGGGGCACTTCCTGCTGTGTGTCTG