Canonical Allele Identifier: CA6169835

Gene: INPPL1

Linked Data

• ClinVar Variation Id: 739475
• ClinVar RCV Id: RCV000915445
• dbSNP Id: rs749984847
• ExAC: 11:71941048 C / T
• gnomAD v2: 11-71941048-C-T
• gnomAD v3: 11-72230004-C-T
• gnomAD v4: 11-72230004-C-T
• MyVariant Identifiers: chr11:g.71941048C>T (hg19) ; chr11:g.72230004C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.72230004C>T , CM000673.2:g.72230004C>T	GRCh38
NC_000011.9:g.71941048C>T , CM000673.1:g.71941048C>T	GRCh37
NC_000011.8:g.71618696C>T	NCBI36
NG_023253.1:g.10167C>T
NG_023253.2:g.10167C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298229.7:c.924C>T MANE Select	ENSP00000298229.2:p.Pro308=
ENST00000298229.6:c.924C>T	ENSP00000298229.2:p.Pro308=
ENST00000538751.5:c.198C>T	ENSP00000444619.1:p.Pro66=
ENST00000540329.5:c.108C>T	ENSP00000440018.1:p.Pro36=
ENST00000541756.5:c.726C>T	ENSP00000446360.2:p.Pro242=
NM_001567.3:c.924C>T	NP_001558.3:p.Pro308=
XM_005273978.3:c.990C>T	XP_005274035.1:p.Pro330=
XM_005273979.3:c.990C>T	XP_005274036.1:p.Pro330=
XM_011544999.1:c.924C>T	XP_011543301.1:p.Pro308=
XM_011545000.1:c.990C>T	XP_011543302.1:p.Pro330=
XM_005273979.4:c.990C>T	XP_005274036.1:p.Pro330=
XM_011544999.2:c.924C>T	XP_011543301.1:p.Pro308=
XM_024448501.1:c.990C>T	XP_024304269.1:p.Pro330=
XM_024448502.1:c.990C>T	XP_024304270.1:p.Pro330=
XM_024448503.1:c.960C>T	XP_024304271.1:p.Pro320=
XM_024448504.1:c.924C>T	XP_024304272.1:p.Pro308=
XM_024448505.1:c.990C>T	XP_024304273.1:p.Pro330=
NM_001567.4:c.924C>T MANE Select	NP_001558.3:p.Pro308=