Canonical Allele Identifier: CA5336711
Community Standard Title: NM_019892.6(INPP5E):c.1629C>G (p.Tyr543Ter)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136431038G>C , CM000671.2:g.136431038G>C GRCh38
NC_000009.11:g.139325490G>C , CM000671.1:g.139325490G>C GRCh37
NC_000009.10:g.138445311G>C NCBI36
NG_016126.1:g.13767C>G

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1629C>G MANE Select NP_063945.2:p.Tyr543Ter
ENST00000371712.4:c.1629C>G MANE Select ENSP00000360777.3:p.Tyr543Ter
NM_001318502.1:c.1626C>G NP_001305431.1:p.Tyr542Ter
NM_001318502.2:c.1626C>G NP_001305431.1:p.Tyr542Ter
NM_019892.4:c.1629C>G NP_063945.2:p.Tyr543Ter
NM_019892.5:c.1629C>G NP_063945.2:p.Tyr543Ter
ENST00000371712.3:c.1629C>G ENSP00000360777.3:p.Tyr543Ter
ENST00000674693.1:n.146C>G
ENST00000676019.1:c.1527C>G ENSP00000501984.1:p.Tyr509Ter
XM_005266094.2:c.1626C>G XP_005266151.1:p.Tyr542Ter
XM_017014926.1:c.1629C>G XP_016870415.1:p.Tyr543Ter
XR_929828.2:n.2234C>G