Canonical Allele Identifier: CA5336632

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136429749G>A , CM000671.2:g.136429749G>A	GRCh38
NC_000009.11:g.139324201G>A , CM000671.1:g.139324201G>A	GRCh37
NC_000009.10:g.138444022G>A	NCBI36
NG_016126.1:g.15056C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_019892.6:c.1861C>T MANE Select	NP_063945.2:p.Arg621Trp
ENST00000371712.4:c.1861C>T MANE Select	ENSP00000360777.3:p.Arg621Trp
NM_001318502.1:c.1858C>T	NP_001305431.1:p.Arg620Trp
NM_001318502.2:c.1858C>T	NP_001305431.1:p.Arg620Trp
NM_019892.4:c.1861C>T	NP_063945.2:p.Arg621Trp
NM_019892.5:c.1861C>T	NP_063945.2:p.Arg621Trp
ENST00000371712.3:c.1861C>T	ENSP00000360777.3:p.Arg621Trp
ENST00000676019.1:c.1759C>T	ENSP00000501984.1:p.Arg587Trp
XM_005266094.2:c.1858C>T	XP_005266151.1:p.Arg620Trp
XM_017014926.1:c.*5C>T	XP_016870415.1:n.*5C>T
XR_929828.2:n.2466C>T