Canonical Allele Identifier: CA600085038

Gene: INPPL1

Linked Data

• dbSNP Id: rs1432480417
• gnomAD v2: 11-71935921-G-C
• MyVariant Identifiers: chr11:g.71935921G>C (hg19) ; chr11:g.72224877G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72224877G>C , CM000673.2:g.72224877G>C	GRCh38
NC_000011.9:g.71935921G>C , CM000673.1:g.71935921G>C	GRCh37
NC_000011.8:g.71613569G>C	NCBI36
NG_023253.1:g.5040G>C
NG_023253.2:g.5040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.-108G>C MANE Select	ENSP00000298229.2:n.-108G>C
ENST00000298229.6:c.-108G>C	ENSP00000298229.2:n.-108G>C
ENST00000540973.1:c.-108G>C	ENSP00000440904.1:n.-108G>C
ENST00000543234.1:c.-108G>C	ENSP00000440512.1:n.-108G>C
NM_001567.3:c.-108G>C	NP_001558.3:n.-108G>C
XM_005273978.3:c.-108G>C	XP_005274035.1:n.-108G>C
XM_005273979.3:c.-108G>C	XP_005274036.1:n.-108G>C
XM_011544999.1:c.-108G>C	XP_011543301.1:n.-108G>C
XM_011545000.1:c.-108G>C	XP_011543302.1:n.-108G>C
XM_005273979.4:c.-108G>C	XP_005274036.1:n.-108G>C
XM_011544999.2:c.-108G>C	XP_011543301.1:n.-108G>C
XM_024448501.1:c.-108G>C	XP_024304269.1:n.-108G>C
XM_024448502.1:c.-108G>C	XP_024304270.1:n.-108G>C
XM_024448503.1:c.-229G>C	XP_024304271.1:n.-229G>C
XM_024448504.1:c.-108G>C	XP_024304272.1:n.-108G>C
XM_024448505.1:c.-108G>C	XP_024304273.1:n.-108G>C
NM_001567.4:c.-108G>C MANE Select	NP_001558.3:n.-108G>C