Canonical Allele Identifier: CA2187894695
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74890554_74890574delinsAGTATGCCTGGGGGAAGATGG , CM000677.2:g.74890554_74890574delinsAGTATGCCTGGGGGAAGATGG GRCh38
NC_000015.9:g.75182895_75182915delinsAGTATGCCTGGGGGAAGATGG , CM000677.1:g.75182895_75182915delinsAGTATGCCTGGGGGAAGATGG GRCh37
NC_000015.8:g.72969948_72969968delinsAGTATGCCTGGGGGAAGATGG NCBI36
NG_008921.1:g.5486_5506delinsAGTATGCCTGGGGGAAGATGG

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.44_64delinsAGTATGCCTGGGGGAAGATGG MANE Select ENSP00000318318.6:p.Gln15=
ENST00000323744.10:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000318192.6:p.Gln15=
ENST00000352410.8:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000318318.6:p.Gln15=
ENST00000535694.5:c.-7+465_-7+485delinsAGTATGCCTGGGGGAAGATGG ENSP00000440447.1:n.-7+465_-7+485delinsAG...
ENST00000561470.5:c.156_176delinsAGTATGCCTGGGGGAAGATGG ENSP00000454267.1:p.Ala52=
ENST00000562606.5:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
ENST00000562800.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000457619.1:p.Gln15=
ENST00000563422.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000457885.1:p.Gln15=
ENST00000563786.5:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
ENST00000564003.5:c.-7+465_-7+485delinsAGTATGCCTGGGGGAAGATGG ENSP00000454312.1:n.-7+465_-7+485delinsAG...
ENST00000564633.5:c.-15-2_4delinsAGTATGCCTGGGGGAAGATGG
ENST00000565576.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000454619.1:p.Gln15=
ENST00000566377.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000455405.1:p.Gln15=
ENST00000567116.5:n.75_95delinsAGTATGCCTGGGGGAAGATGG
ENST00000567132.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000455972.1:p.Gln15=
ENST00000567177.1:c.5_25delinsAGTATGCCTGGGGGAAGATGG ENSP00000457013.1:p.Gln2=
ENST00000567570.5:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
ENST00000568303.1:n.161_181delinsAGTATGCCTGGGGGAAGATGG
ENST00000568828.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000455065.1:p.Gln15=
ENST00000568840.1:n.153_173delinsAGTATGCCTGGGGGAAGATGG
ENST00000568907.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000457494.1:p.Gln15=
ENST00000569233.5:c.44_64delinsAGTATGCCTGGGGGAAGATGG ENSP00000454622.1:p.Gln15=
ENST00000569931.5:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
NM_001289155.1:c.44_64delinsAGTATGCCTGGGGGAAGATGG NP_001276084.1:p.Gln15=
NM_001289156.1:c.-7+465_-7+485delinsAGTATGCCTGGGGGAAGATGG NP_001276085.1:n.-7+465_-7+485delinsAGTAT...
NM_001289157.1:c.44_64delinsAGTATGCCTGGGGGAAGATGG NP_001276086.1:p.Gln15=
NM_002435.2:c.44_64delinsAGTATGCCTGGGGGAAGATGG NP_002426.1:p.Gln15=
XM_011521592.1:c.32_52delinsAGTATGCCTGGGGGAAGATGG XP_011519894.1:p.Gln11=
XM_011521593.1:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
NM_001330372.1:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
XM_017022208.1:c.-17_4delinsAGTATGCCTGGGGGAAGATGG
XM_017022209.2:c.-7+465_-7+485delinsAGTATGCCTGGGGGAAGATGG XP_016877698.1:n.-7+465_-7+485delinsAGTAT...
NM_002435.3:c.44_64delinsAGTATGCCTGGGGGAAGATGG MANE Select NP_002426.1:p.Gln15=
NM_001289155.2:c.44_64delinsAGTATGCCTGGGGGAAGATGG NP_001276084.1:p.Gln15=
NM_001289156.2:c.-7+465_-7+485delinsAGTATGCCTGGGGGAAGATGG NP_001276085.1:n.-7+465_-7+485delinsAGTAT...
NM_001289157.2:c.44_64delinsAGTATGCCTGGGGGAAGATGG NP_001276086.1:p.Gln15=
NM_001330372.2:c.-17_4delinsAGTATGCCTGGGGGAAGATGG