Canonical Allele Identifier: CA279841
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 218094
ClinVar RCV Id: RCV000202323
dbSNP Id: rs863225086

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74897663A>G , CM000677.2:g.74897663A>G GRCh38
NC_000015.9:g.75190004A>G , CM000677.1:g.75190004A>G GRCh37
NC_000015.8:g.72977057A>G NCBI36
NG_008921.1:g.12595A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.1205A>G MANE Select ENSP00000318318.6:p.Glu402Gly
ENST00000323744.10:c.1022A>G ENSP00000318192.6:p.Glu341Gly
ENST00000352410.8:c.1205A>G ENSP00000318318.6:p.Glu402Gly
ENST00000535694.5:c.1055A>G ENSP00000440447.1:p.Glu352Gly
ENST00000563786.5:c.1145A>G ENSP00000455241.1:p.Glu382Gly
ENST00000566377.5:c.*132A>G ENSP00000455405.1:n.*132A>G
ENST00000566556.1:n.2230A>G
ENST00000567177.1:c.774A>G ENSP00000457013.1:n.774A>G
NM_001289155.1:c.*132A>G NP_001276084.1:n.*132A>G
NM_001289156.1:c.1055A>G NP_001276085.1:p.Glu352Gly
NM_001289157.1:c.1022A>G NP_001276086.1:p.Glu341Gly
NM_002435.2:c.1205A>G NP_002426.1:p.Glu402Gly
XM_011521592.1:c.1193A>G XP_011519894.1:p.Glu398Gly
XM_011521593.1:c.1145A>G XP_011519895.1:p.Glu382Gly
NM_001330372.1:c.1145A>G NP_001317301.1:p.Glu382Gly
XM_017022208.1:c.*132A>G XP_016877697.1:n.*132A>G
XM_017022209.2:c.*132A>G XP_016877698.1:n.*132A>G
NM_002435.3:c.1205A>G MANE Select NP_002426.1:p.Glu402Gly
NM_001289155.2:c.*132A>G NP_001276084.1:n.*132A>G
NM_001289156.2:c.1055A>G NP_001276085.1:p.Glu352Gly
NM_001289157.2:c.1022A>G NP_001276086.1:p.Glu341Gly
NM_001330372.2:c.1145A>G NP_001317301.1:p.Glu382Gly