Canonical Allele Identifier: CA381722825

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71940991G>C (hg19) ; chr11:g.72229947G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229947G>C , CM000673.2:g.72229947G>C	GRCh38
NC_000011.9:g.71940991G>C , CM000673.1:g.71940991G>C	GRCh37
NC_000011.8:g.71618639G>C	NCBI36
NG_023253.1:g.10110G>C
NG_023253.2:g.10110G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.867G>C MANE Select	ENSP00000298229.2:p.Met289Ile
ENST00000298229.6:c.867G>C	ENSP00000298229.2:p.Met289Ile
ENST00000538751.5:c.141G>C	ENSP00000444619.1:p.Met47Ile
ENST00000540329.5:c.51G>C	ENSP00000440018.1:p.Met17Ile
ENST00000541756.5:c.669G>C	ENSP00000446360.2:p.Met223Ile
NM_001567.3:c.867G>C	NP_001558.3:p.Met289Ile
XM_005273978.3:c.933G>C	XP_005274035.1:p.Met311Ile
XM_005273979.3:c.933G>C	XP_005274036.1:p.Met311Ile
XM_011544999.1:c.867G>C	XP_011543301.1:p.Met289Ile
XM_011545000.1:c.933G>C	XP_011543302.1:p.Met311Ile
XM_005273979.4:c.933G>C	XP_005274036.1:p.Met311Ile
XM_011544999.2:c.867G>C	XP_011543301.1:p.Met289Ile
XM_024448501.1:c.933G>C	XP_024304269.1:p.Met311Ile
XM_024448502.1:c.933G>C	XP_024304270.1:p.Met311Ile
XM_024448503.1:c.903G>C	XP_024304271.1:p.Met301Ile
XM_024448504.1:c.867G>C	XP_024304272.1:p.Met289Ile
XM_024448505.1:c.933G>C	XP_024304273.1:p.Met311Ile
NM_001567.4:c.867G>C MANE Select	NP_001558.3:p.Met289Ile