Canonical Allele Identifier: CA375569072
Community Standard Title: NM_019892.6(INPP5E):c.430C>G (p.Arg144Gly)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136438990G>C , CM000671.2:g.136438990G>C GRCh38
NC_000009.11:g.139333442G>C , CM000671.1:g.139333442G>C GRCh37
NC_000009.10:g.138453263G>C NCBI36
NG_016126.1:g.5815C>G

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.430C>G MANE Select NP_063945.2:p.Arg144Gly
ENST00000371712.4:c.430C>G MANE Select ENSP00000360777.3:p.Arg144Gly
NM_001318502.1:c.430C>G NP_001305431.1:p.Arg144Gly
NM_001318502.2:c.430C>G NP_001305431.1:p.Arg144Gly
NM_019892.4:c.430C>G NP_063945.2:p.Arg144Gly
NM_019892.5:c.430C>G NP_063945.2:p.Arg144Gly
ENST00000371712.3:c.430C>G ENSP00000360777.3:p.Arg144Gly
ENST00000635815.1:n.834C>G
ENST00000676019.1:c.430C>G ENSP00000501984.1:p.Arg144Gly
XM_005266094.2:c.430C>G XP_005266151.1:p.Arg144Gly
XM_017014926.1:c.430C>G XP_016870415.1:p.Arg144Gly
XR_929828.1:n.870C>G
XR_929828.2:n.872C>G