Canonical Allele Identifier: CA895953282

Gene: INPP4A

Linked Data

• dbSNP Id: rs12617721
• MyVariant Identifiers: chr2:g.99083892A>G (hg19) ; chr2:g.98467429A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.98467429A>G , CM000664.2:g.98467429A>G	GRCh38
NC_000002.11:g.99083892A>G , CM000664.1:g.99083892A>G	GRCh37
NC_000002.10:g.98450324A>G	NCBI36
NG_029890.1:g.27572A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706935.1:c.-166+22344A>G	ENSP00000516656.1:n.-166+22344A>G
ENST00000409851.8:c.-166+22344A>G MANE Select	ENSP00000386777.4:n.-166+22344A>G
ENST00000074304.9:c.-166+22344A>G	ENSP00000074304.5:n.-166+22344A>G
ENST00000409016.8:c.-166+22344A>G	ENSP00000386704.3:n.-166+22344A>G
ENST00000409463.5:c.-166+22344A>G	ENSP00000386329.1:n.-166+22344A>G
ENST00000409540.7:c.-166+22344A>G	ENSP00000387294.3:n.-166+22344A>G
ENST00000409851.7:c.-166+22344A>G	ENSP00000386777.3:n.-166+22344A>G
NM_001134224.1:c.-166+22344A>G	NP_001127696.1:n.-166+22344A>G
NM_001134225.1:c.-166+22344A>G	NP_001127697.1:n.-166+22344A>G
NM_001566.2:c.-166+22344A>G	NP_001557.1:n.-166+22344A>G
NM_004027.2:c.-166+22344A>G	NP_004018.1:n.-166+22344A>G
XM_006712499.2:c.-166+22344A>G	XP_006712562.1:n.-166+22344A>G
XM_006712500.2:c.-166+22344A>G	XP_006712563.1:n.-166+22344A>G
XM_006712501.2:c.-166+22344A>G	XP_006712564.1:n.-166+22344A>G
XM_006712502.2:c.-166+22344A>G	XP_006712565.1:n.-166+22344A>G
XM_006712503.2:c.-166+22344A>G	XP_006712566.1:n.-166+22344A>G
XM_006712504.2:c.-166+22344A>G	XP_006712567.1:n.-166+22344A>G
XM_006712505.2:c.-166+22344A>G	XP_006712568.1:n.-166+22344A>G
XM_006712506.2:c.-166+22344A>G	XP_006712569.1:n.-166+22344A>G
XM_006712507.2:c.-166+22344A>G	XP_006712570.1:n.-166+22344A>G
XM_006712508.2:c.-166+22344A>G	XP_006712571.1:n.-166+22344A>G
XM_011511122.1:c.-166+22344A>G	XP_011509424.1:n.-166+22344A>G
XM_011511123.1:c.-166+22344A>G	XP_011509425.1:n.-166+22344A>G
XM_011511124.1:c.-166+22344A>G	XP_011509426.1:n.-166+22344A>G
XR_922915.1:n.228+22344A>G
XR_922916.1:n.228+22344A>G
NM_001351424.1:c.-166+22774A>G	NP_001338353.1:n.-166+22774A>G
NM_001351425.1:c.-166+22344A>G	NP_001338354.1:n.-166+22344A>G
NM_001351426.1:c.-166+21279A>G	NP_001338355.1:n.-166+21279A>G
NM_001351427.1:c.-166+21279A>G	NP_001338356.1:n.-166+21279A>G
NM_001351428.1:c.-166+21279A>G	NP_001338357.1:n.-166+21279A>G
NM_001351429.1:c.-166+21279A>G	NP_001338358.1:n.-166+21279A>G
XM_006712499.3:c.-166+22344A>G	XP_006712562.1:n.-166+22344A>G
XM_006712500.3:c.-166+22344A>G	XP_006712563.1:n.-166+22344A>G
XM_006712501.3:c.-166+22344A>G	XP_006712564.1:n.-166+22344A>G
XM_006712502.3:c.-166+22344A>G	XP_006712565.1:n.-166+22344A>G
XM_006712503.3:c.-166+22344A>G	XP_006712566.1:n.-166+22344A>G
XM_006712504.3:c.-166+22344A>G	XP_006712567.1:n.-166+22344A>G
XM_006712505.3:c.-166+22344A>G	XP_006712568.1:n.-166+22344A>G
XM_006712506.3:c.-166+22344A>G	XP_006712569.1:n.-166+22344A>G
XM_006712508.3:c.-166+22344A>G	XP_006712571.1:n.-166+22344A>G
XM_011511122.2:c.-166+22344A>G	XP_011509424.1:n.-166+22344A>G
XM_011511123.2:c.-166+22344A>G	XP_011509425.1:n.-166+22344A>G
XM_011511124.2:c.-166+22344A>G	XP_011509426.1:n.-166+22344A>G
XM_017003994.1:c.-166+22344A>G	XP_016859483.1:n.-166+22344A>G
XM_017003995.1:c.-166+22344A>G	XP_016859484.1:n.-166+22344A>G
XM_017003996.1:c.-166+22344A>G	XP_016859485.1:n.-166+22344A>G
XM_017004000.1:c.-166+22344A>G	XP_016859489.1:n.-166+22344A>G
XM_017004001.1:c.-166+22344A>G	XP_016859490.1:n.-166+22344A>G
XM_017004003.1:c.-166+22344A>G	XP_016859492.1:n.-166+22344A>G
XM_024452876.1:c.-166+22774A>G	XP_024308644.1:n.-166+22774A>G
XR_001738737.1:n.223+22344A>G
XR_001738738.1:n.223+22344A>G
XR_922915.2:n.223+22344A>G
XR_922916.2:n.223+22344A>G
NM_001134225.2:c.-166+22344A>G MANE Select	NP_001127697.1:n.-166+22344A>G
NM_001351425.2:c.-166+22344A>G	NP_001338354.1:n.-166+22344A>G
NM_004027.3:c.-166+22344A>G	NP_004018.1:n.-166+22344A>G
NM_001134224.2:c.-166+22344A>G	NP_001127696.1:n.-166+22344A>G
NM_001351426.2:c.-166+21279A>G	NP_001338355.1:n.-166+21279A>G
NM_001351427.2:c.-166+21279A>G	NP_001338356.1:n.-166+21279A>G
NM_001351428.2:c.-166+21279A>G	NP_001338357.1:n.-166+21279A>G
NM_001351429.2:c.-166+21279A>G	NP_001338358.1:n.-166+21279A>G