Canonical Allele Identifier: CA861054691

Gene: INPP5E

Linked Data

• dbSNP Id: rs979010697
• gnomAD v3: 9-136428777-C-G
• gnomAD v4: 9-136428777-C-G
• MyVariant Identifiers: chr9:g.139323229C>G (hg19) ; chr9:g.136428777C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428777C>G , CM000671.2:g.136428777C>G	GRCh38
NC_000009.11:g.139323229C>G , CM000671.1:g.139323229C>G	GRCh37
NC_000009.10:g.138443050C>G	NCBI36
NG_016126.1:g.16028G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*898G>C MANE Select	ENSP00000360777.3:n.*898G>C
ENST00000676019.1:c.*898G>C	ENSP00000501984.1:n.*898G>C
ENST00000371712.3:c.*898G>C	ENSP00000360777.3:n.*898G>C
NM_019892.4:c.*898G>C	NP_063945.2:n.*898G>C
XM_005266094.2:c.*898G>C	XP_005266151.1:n.*898G>C
NM_001318502.1:c.*898G>C	NP_001305431.1:n.*898G>C
NM_019892.5:c.*898G>C	NP_063945.2:n.*898G>C
XM_017014926.1:c.*977G>C	XP_016870415.1:n.*977G>C
NM_019892.6:c.*898G>C MANE Select	NP_063945.2:n.*898G>C
NM_001318502.2:c.*898G>C	NP_001305431.1:n.*898G>C