Canonical Allele Identifier: CA381722883

Gene: INPPL1

Linked Data

• COSMIC: COSM5630253
• MyVariant Identifiers: chr11:g.71940996C>G (hg19) ; chr11:g.72229952C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72229952C>G , CM000673.2:g.72229952C>G	GRCh38
NC_000011.9:g.71940996C>G , CM000673.1:g.71940996C>G	GRCh37
NC_000011.8:g.71618644C>G	NCBI36
NG_023253.1:g.10115C>G
NG_023253.2:g.10115C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.872C>G MANE Select	ENSP00000298229.2:p.Ser291Cys
ENST00000298229.6:c.872C>G	ENSP00000298229.2:p.Ser291Cys
ENST00000538751.5:c.146C>G	ENSP00000444619.1:p.Ser49Cys
ENST00000540329.5:c.56C>G	ENSP00000440018.1:p.Ser19Cys
ENST00000541756.5:c.674C>G	ENSP00000446360.2:p.Ser225Cys
NM_001567.3:c.872C>G	NP_001558.3:p.Ser291Cys
XM_005273978.3:c.938C>G	XP_005274035.1:p.Ser313Cys
XM_005273979.3:c.938C>G	XP_005274036.1:p.Ser313Cys
XM_011544999.1:c.872C>G	XP_011543301.1:p.Ser291Cys
XM_011545000.1:c.938C>G	XP_011543302.1:p.Ser313Cys
XM_005273979.4:c.938C>G	XP_005274036.1:p.Ser313Cys
XM_011544999.2:c.872C>G	XP_011543301.1:p.Ser291Cys
XM_024448501.1:c.938C>G	XP_024304269.1:p.Ser313Cys
XM_024448502.1:c.938C>G	XP_024304270.1:p.Ser313Cys
XM_024448503.1:c.908C>G	XP_024304271.1:p.Ser303Cys
XM_024448504.1:c.872C>G	XP_024304272.1:p.Ser291Cys
XM_024448505.1:c.938C>G	XP_024304273.1:p.Ser313Cys
NM_001567.4:c.872C>G MANE Select	NP_001558.3:p.Ser291Cys