Canonical Allele Identifier: CA201636985

Gene: INPP5E

Linked Data

• dbSNP Id: rs994805971
• MyVariant Identifiers: chr9:g.136428686T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428686T>G , CM000671.2:g.136428686T>G	GRCh38
NC_000009.11:g.139323138T>G , CM000671.1:g.139323138T>G	GRCh37
NC_000009.10:g.138442959T>G	NCBI36
NG_016126.1:g.16119A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*989A>C MANE Select	ENSP00000360777.3:n.*989A>C
ENST00000676019.1:c.*989A>C	ENSP00000501984.1:n.*989A>C
ENST00000371712.3:c.*989A>C	ENSP00000360777.3:n.*989A>C
NM_019892.4:c.*989A>C	NP_063945.2:n.*989A>C
XM_005266094.2:c.*989A>C	XP_005266151.1:n.*989A>C
NM_001318502.1:c.*989A>C	NP_001305431.1:n.*989A>C
NM_019892.5:c.*989A>C	NP_063945.2:n.*989A>C
XM_017014926.1:c.*1068A>C	XP_016870415.1:n.*1068A>C
NM_019892.6:c.*989A>C MANE Select	NP_063945.2:n.*989A>C
NM_001318502.2:c.*989A>C	NP_001305431.1:n.*989A>C