Canonical Allele Identifier: CA6170345

Gene: INPPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72234614C>T , CM000673.2:g.72234614C>T	GRCh38
NC_000011.9:g.71945658C>T , CM000673.1:g.71945658C>T	GRCh37
NC_000011.8:g.71623306C>T	NCBI36
NG_023253.1:g.14777C>T
NG_023253.2:g.14777C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001567.4:c.2414C>T MANE Select	NP_001558.3:p.Thr805Met
ENST00000298229.7:c.2414C>T MANE Select	ENSP00000298229.2:p.Thr805Met
NM_001567.3:c.2414C>T	NP_001558.3:p.Thr805Met
ENST00000298229.6:c.2414C>T	ENSP00000298229.2:p.Thr805Met
ENST00000535985.1:c.267C>T
ENST00000538751.5:c.1688C>T	ENSP00000444619.1:p.Thr563Met
ENST00000541303.5:n.1020C>T
ENST00000541756.5:c.2216C>T	ENSP00000446360.2:p.Thr739Met
ENST00000545355.5:n.699C>T
XM_005273978.3:c.2480C>T	XP_005274035.1:p.Thr827Met
XM_005273979.3:c.2480C>T	XP_005274036.1:p.Thr827Met
XM_005273979.4:c.2480C>T	XP_005274036.1:p.Thr827Met
XM_011544999.1:c.2414C>T	XP_011543301.1:p.Thr805Met
XM_011544999.2:c.2414C>T	XP_011543301.1:p.Thr805Met
XM_011545000.1:c.2480C>T	XP_011543302.1:p.Thr827Met
XM_024448501.1:c.2612C>T	XP_024304269.1:p.Thr871Met
XM_024448502.1:c.2612C>T	XP_024304270.1:p.Thr871Met
XM_024448503.1:c.2582C>T	XP_024304271.1:p.Thr861Met
XM_024448504.1:c.2546C>T	XP_024304272.1:p.Thr849Met
XM_024448505.1:c.2612C>T	XP_024304273.1:p.Thr871Met