Canonical Allele Identifier: CA6170176

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72232916C>A , CM000673.2:g.72232916C>A	GRCh38
NC_000011.9:g.71943960C>A , CM000673.1:g.71943960C>A	GRCh37
NC_000011.8:g.71621608C>A	NCBI36
NG_023253.1:g.13079C>A
NG_023253.2:g.13079C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.1893C>A MANE Select	NP_001558.3:p.Leu631=
ENST00000298229.7:c.1893C>A MANE Select	ENSP00000298229.2:p.Leu631=
NM_001567.3:c.1893C>A	NP_001558.3:p.Leu631=
ENST00000298229.6:c.1893C>A	ENSP00000298229.2:p.Leu631=
ENST00000538751.5:c.1167C>A	ENSP00000444619.1:p.Leu389=
ENST00000541303.5:n.499C>A
ENST00000541756.5:c.1695C>A	ENSP00000446360.2:p.Leu565=
ENST00000545355.5:n.46C>A
XM_005273978.3:c.1959C>A	XP_005274035.1:p.Leu653=
XM_005273979.3:c.1959C>A	XP_005274036.1:p.Leu653=
XM_005273979.4:c.1959C>A	XP_005274036.1:p.Leu653=
XM_011544999.1:c.1893C>A	XP_011543301.1:p.Leu631=
XM_011544999.2:c.1893C>A	XP_011543301.1:p.Leu631=
XM_011545000.1:c.1959C>A	XP_011543302.1:p.Leu653=
XM_024448501.1:c.1959C>A	XP_024304269.1:p.Leu653=
XM_024448502.1:c.1959C>A	XP_024304270.1:p.Leu653=
XM_024448503.1:c.1929C>A	XP_024304271.1:p.Leu643=
XM_024448504.1:c.1893C>A	XP_024304272.1:p.Leu631=
XM_024448505.1:c.1959C>A	XP_024304273.1:p.Leu653=