Canonical Allele Identifier: CA600242952

Gene: INPPL1

Linked Data

• dbSNP Id: rs1254260482
• gnomAD v2: 11-71936377-AGGGGCACTTCCTGCTGTGTGTCTG-A
• gnomAD v3: 11-72225333-AGGGGCACTTCCTGCTGTGTGTCTG-A
• gnomAD v4: 11-72225333-AGGGGCACTTCCTGCTGTGTGTCTG-A
• MyVariant Identifiers: chr11:g.71936378_71936401del (hg19) ; chr11:g.72225334_72225357del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72225343_72225366del , CM000673.2:g.72225343_72225366del	GRCh38
NC_000011.9:g.71936387_71936410del , CM000673.1:g.71936387_71936410del	GRCh37
NC_000011.8:g.71614035_71614058del	NCBI36
NG_023253.1:g.5506_5529del
NG_023253.2:g.5506_5529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.182+177_182+200del MANE Select	ENSP00000298229.2:n.182+177_182+200del
ENST00000298229.6:c.182+177_182+200del	ENSP00000298229.2:n.182+177_182+200del
ENST00000541544.1:n.98+177_98+200del
NM_001567.3:c.182+177_182+200del	NP_001558.3:n.182+177_182+200del
XM_005273978.3:c.182+177_182+200del	XP_005274035.1:n.182+177_182+200del
XM_005273979.3:c.182+177_182+200del	XP_005274036.1:n.182+177_182+200del
XM_011544999.1:c.182+177_182+200del	XP_011543301.1:n.182+177_182+200del
XM_011545000.1:c.182+177_182+200del	XP_011543302.1:n.182+177_182+200del
XM_005273979.4:c.182+177_182+200del	XP_005274036.1:n.182+177_182+200del
XM_011544999.2:c.182+177_182+200del	XP_011543301.1:n.182+177_182+200del
XM_024448501.1:c.182+177_182+200del	XP_024304269.1:n.182+177_182+200del
XM_024448502.1:c.182+177_182+200del	XP_024304270.1:n.182+177_182+200del
XM_024448503.1:c.62-107_62-84del	XP_024304271.1:n.62-107_62-84del
XM_024448504.1:c.182+177_182+200del	XP_024304272.1:n.182+177_182+200del
XM_024448505.1:c.182+177_182+200del	XP_024304273.1:n.182+177_182+200del
NM_001567.4:c.182+177_182+200del MANE Select	NP_001558.3:n.182+177_182+200del