Canonical Allele Identifier: CA375560310
Community Standard Title: NM_019892.6(INPP5E):c.1844T>G (p.Leu615Ter)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136429766A>C , CM000671.2:g.136429766A>C GRCh38
NC_000009.11:g.139324218A>C , CM000671.1:g.139324218A>C GRCh37
NC_000009.10:g.138444039A>C NCBI36
NG_016126.1:g.15039T>G

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1844T>G MANE Select NP_063945.2:p.Leu615Ter
ENST00000371712.4:c.1844T>G MANE Select ENSP00000360777.3:p.Leu615Ter
NM_001318502.1:c.1841T>G NP_001305431.1:p.Leu614Ter
NM_001318502.2:c.1841T>G NP_001305431.1:p.Leu614Ter
NM_019892.4:c.1844T>G NP_063945.2:p.Leu615Ter
NM_019892.5:c.1844T>G NP_063945.2:p.Leu615Ter
ENST00000371712.3:c.1844T>G ENSP00000360777.3:p.Leu615Ter
ENST00000676019.1:c.1742T>G ENSP00000501984.1:p.Leu581Ter
XM_005266094.2:c.1841T>G XP_005266151.1:p.Leu614Ter
XM_017014926.1:c.1803-6T>G XP_016870415.1:n.1803-6T>G
XR_929828.2:n.2449T>G