Canonical Allele Identifier: CA2692611934

Gene: INPP5E

Linked Data

• gnomAD v4: 9-136430419-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136430419G>C , CM000671.2:g.136430419G>C	GRCh38
NC_000009.11:g.139324871G>C , CM000671.1:g.139324871G>C	GRCh37
NC_000009.10:g.138444692G>C	NCBI36
NG_016126.1:g.14386C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.1666-6C>G MANE Select	ENSP00000360777.3:n.1666-6C>G
ENST00000674693.1:n.183-6C>G
ENST00000676019.1:c.1564-6C>G	ENSP00000501984.1:n.1564-6C>G
ENST00000371712.3:c.1666-6C>G	ENSP00000360777.3:n.1666-6C>G
NM_019892.4:c.1666-6C>G	NP_063945.2:n.1666-6C>G
XM_005266094.2:c.1663-6C>G	XP_005266151.1:n.1663-6C>G
NM_001318502.1:c.1663-6C>G	NP_001305431.1:n.1663-6C>G
NM_019892.5:c.1666-6C>G	NP_063945.2:n.1666-6C>G
XM_017014926.1:c.1666-6C>G	XP_016870415.1:n.1666-6C>G
XR_929828.2:n.2271-6C>G
NM_019892.6:c.1666-6C>G MANE Select	NP_063945.2:n.1666-6C>G
NM_001318502.2:c.1663-6C>G	NP_001305431.1:n.1663-6C>G