Canonical Allele Identifier: CA381722997

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71941010G>T (hg19) ; chr11:g.72229966G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229966G>T , CM000673.2:g.72229966G>T	GRCh38
NC_000011.9:g.71941010G>T , CM000673.1:g.71941010G>T	GRCh37
NC_000011.8:g.71618658G>T	NCBI36
NG_023253.1:g.10129G>T
NG_023253.2:g.10129G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.886G>T MANE Select	ENSP00000298229.2:p.Ala296Ser
ENST00000298229.6:c.886G>T	ENSP00000298229.2:p.Ala296Ser
ENST00000538751.5:c.160G>T	ENSP00000444619.1:p.Ala54Ser
ENST00000540329.5:c.70G>T	ENSP00000440018.1:p.Ala24Ser
ENST00000541756.5:c.688G>T	ENSP00000446360.2:p.Ala230Ser
NM_001567.3:c.886G>T	NP_001558.3:p.Ala296Ser
XM_005273978.3:c.952G>T	XP_005274035.1:p.Ala318Ser
XM_005273979.3:c.952G>T	XP_005274036.1:p.Ala318Ser
XM_011544999.1:c.886G>T	XP_011543301.1:p.Ala296Ser
XM_011545000.1:c.952G>T	XP_011543302.1:p.Ala318Ser
XM_005273979.4:c.952G>T	XP_005274036.1:p.Ala318Ser
XM_011544999.2:c.886G>T	XP_011543301.1:p.Ala296Ser
XM_024448501.1:c.952G>T	XP_024304269.1:p.Ala318Ser
XM_024448502.1:c.952G>T	XP_024304270.1:p.Ala318Ser
XM_024448503.1:c.922G>T	XP_024304271.1:p.Ala308Ser
XM_024448504.1:c.886G>T	XP_024304272.1:p.Ala296Ser
XM_024448505.1:c.952G>T	XP_024304273.1:p.Ala318Ser
NM_001567.4:c.886G>T MANE Select	NP_001558.3:p.Ala296Ser