Canonical Allele Identifier: CA1981895573

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225297_72225298delinsGA , CM000673.2:g.72225297_72225298delinsGA	GRCh38
NC_000011.9:g.71936341_71936342delinsGA , CM000673.1:g.71936341_71936342delinsGA	GRCh37
NC_000011.8:g.71613989_71613990delinsGA	NCBI36
NG_023253.1:g.5460_5461delinsGA
NG_023253.2:g.5460_5461delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+131_182+132delinsGA MANE Select	ENSP00000298229.2:n.182+131_182+132delinsGA
ENST00000298229.6:c.182+131_182+132delinsGA	ENSP00000298229.2:n.182+131_182+132delinsGA
ENST00000541544.1:n.98+131_98+132delinsGA
NM_001567.3:c.182+131_182+132delinsGA	NP_001558.3:n.182+131_182+132delinsGA
XM_005273978.3:c.182+131_182+132delinsGA	XP_005274035.1:n.182+131_182+132delinsGA
XM_005273979.3:c.182+131_182+132delinsGA	XP_005274036.1:n.182+131_182+132delinsGA
XM_011544999.1:c.182+131_182+132delinsGA	XP_011543301.1:n.182+131_182+132delinsGA
XM_011545000.1:c.182+131_182+132delinsGA	XP_011543302.1:n.182+131_182+132delinsGA
XM_005273979.4:c.182+131_182+132delinsGA	XP_005274036.1:n.182+131_182+132delinsGA
XM_011544999.2:c.182+131_182+132delinsGA	XP_011543301.1:n.182+131_182+132delinsGA
XM_024448501.1:c.182+131_182+132delinsGA	XP_024304269.1:n.182+131_182+132delinsGA
XM_024448502.1:c.182+131_182+132delinsGA	XP_024304270.1:n.182+131_182+132delinsGA
XM_024448503.1:c.61+131_61+132delinsGA	XP_024304271.1:n.61+131_61+132delinsGA
XM_024448504.1:c.182+131_182+132delinsGA	XP_024304272.1:n.182+131_182+132delinsGA
XM_024448505.1:c.182+131_182+132delinsGA	XP_024304273.1:n.182+131_182+132delinsGA
NM_001567.4:c.182+131_182+132delinsGA MANE Select	NP_001558.3:n.182+131_182+132delinsGA