Canonical Allele Identifier: CA861054620

Gene: INPP5E

Linked Data

• dbSNP Id: rs1467683377
• gnomAD v3: 9-136428696-T-C
• gnomAD v4: 9-136428696-T-C
• MyVariant Identifiers: chr9:g.139323148T>C (hg19) ; chr9:g.136428696T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428696T>C , CM000671.2:g.136428696T>C	GRCh38
NC_000009.11:g.139323148T>C , CM000671.1:g.139323148T>C	GRCh37
NC_000009.10:g.138442969T>C	NCBI36
NG_016126.1:g.16109A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*979A>G MANE Select	ENSP00000360777.3:n.*979A>G
ENST00000676019.1:c.*979A>G	ENSP00000501984.1:n.*979A>G
ENST00000371712.3:c.*979A>G	ENSP00000360777.3:n.*979A>G
NM_019892.4:c.*979A>G	NP_063945.2:n.*979A>G
XM_005266094.2:c.*979A>G	XP_005266151.1:n.*979A>G
NM_001318502.1:c.*979A>G	NP_001305431.1:n.*979A>G
NM_019892.5:c.*979A>G	NP_063945.2:n.*979A>G
XM_017014926.1:c.*1058A>G	XP_016870415.1:n.*1058A>G
NM_019892.6:c.*979A>G MANE Select	NP_063945.2:n.*979A>G
NM_001318502.2:c.*979A>G	NP_001305431.1:n.*979A>G