Canonical Allele Identifier: CA381724738

Gene: INPPL1

Linked Data

• MyVariant Identifiers: chr11:g.71941291T>G (hg19) ; chr11:g.72230247T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230247T>G , CM000673.2:g.72230247T>G	GRCh38
NC_000011.9:g.71941291T>G , CM000673.1:g.71941291T>G	GRCh37
NC_000011.8:g.71618939T>G	NCBI36
NG_023253.1:g.10410T>G
NG_023253.2:g.10410T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298229.7:c.1066T>G MANE Select	ENSP00000298229.2:p.Trp356Gly
ENST00000298229.6:c.1066T>G	ENSP00000298229.2:p.Trp356Gly
ENST00000538751.5:c.340T>G	ENSP00000444619.1:p.Trp114Gly
ENST00000540329.5:c.250T>G	ENSP00000440018.1:p.Trp84Gly
ENST00000541756.5:c.868T>G	ENSP00000446360.2:p.Trp290Gly
NM_001567.3:c.1066T>G	NP_001558.3:p.Trp356Gly
XM_005273978.3:c.1132T>G	XP_005274035.1:p.Trp378Gly
XM_005273979.3:c.1132T>G	XP_005274036.1:p.Trp378Gly
XM_011544999.1:c.1066T>G	XP_011543301.1:p.Trp356Gly
XM_011545000.1:c.1132T>G	XP_011543302.1:p.Trp378Gly
XM_005273979.4:c.1132T>G	XP_005274036.1:p.Trp378Gly
XM_011544999.2:c.1066T>G	XP_011543301.1:p.Trp356Gly
XM_024448501.1:c.1132T>G	XP_024304269.1:p.Trp378Gly
XM_024448502.1:c.1132T>G	XP_024304270.1:p.Trp378Gly
XM_024448503.1:c.1102T>G	XP_024304271.1:p.Trp368Gly
XM_024448504.1:c.1066T>G	XP_024304272.1:p.Trp356Gly
XM_024448505.1:c.1132T>G	XP_024304273.1:p.Trp378Gly
NM_001567.4:c.1066T>G MANE Select	NP_001558.3:p.Trp356Gly