Canonical Allele Identifier: CA381722820

Gene: INPPL1

Linked Data

• gnomAD v4: 11-72229946-T-C
• MyVariant Identifiers: chr11:g.71940990T>C (hg19) ; chr11:g.72229946T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229946T>C , CM000673.2:g.72229946T>C	GRCh38
NC_000011.9:g.71940990T>C , CM000673.1:g.71940990T>C	GRCh37
NC_000011.8:g.71618638T>C	NCBI36
NG_023253.1:g.10109T>C
NG_023253.2:g.10109T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.866T>C MANE Select	ENSP00000298229.2:p.Met289Thr
ENST00000298229.6:c.866T>C	ENSP00000298229.2:p.Met289Thr
ENST00000538751.5:c.140T>C	ENSP00000444619.1:p.Met47Thr
ENST00000540329.5:c.50T>C	ENSP00000440018.1:p.Met17Thr
ENST00000541756.5:c.668T>C	ENSP00000446360.2:p.Met223Thr
NM_001567.3:c.866T>C	NP_001558.3:p.Met289Thr
XM_005273978.3:c.932T>C	XP_005274035.1:p.Met311Thr
XM_005273979.3:c.932T>C	XP_005274036.1:p.Met311Thr
XM_011544999.1:c.866T>C	XP_011543301.1:p.Met289Thr
XM_011545000.1:c.932T>C	XP_011543302.1:p.Met311Thr
XM_005273979.4:c.932T>C	XP_005274036.1:p.Met311Thr
XM_011544999.2:c.866T>C	XP_011543301.1:p.Met289Thr
XM_024448501.1:c.932T>C	XP_024304269.1:p.Met311Thr
XM_024448502.1:c.932T>C	XP_024304270.1:p.Met311Thr
XM_024448503.1:c.902T>C	XP_024304271.1:p.Met301Thr
XM_024448504.1:c.866T>C	XP_024304272.1:p.Met289Thr
XM_024448505.1:c.932T>C	XP_024304273.1:p.Met311Thr
NM_001567.4:c.866T>C MANE Select	NP_001558.3:p.Met289Thr