Canonical Allele Identifier: CA2187901701
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74896157G= , CM000677.2:g.74896157G= GRCh38
NC_000015.9:g.75188498G= , CM000677.1:g.75188498G= GRCh37
NC_000015.8:g.72975551G= NCBI36
NG_008921.1:g.11089G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.676G= MANE Select ENSP00000318318.6:p.Ala226=
ENST00000323744.10:c.493G= ENSP00000318192.6:p.Ala165=
ENST00000352410.8:c.676G= ENSP00000318318.6:p.Ala226=
ENST00000535694.5:c.526G= ENSP00000440447.1:p.Ala176=
ENST00000561470.5:c.*572G= ENSP00000454267.1:n.*572G=
ENST00000562606.5:c.616G= ENSP00000457020.1:p.Ala206=
ENST00000562800.5:c.256-1382G= ENSP00000457619.1:n.256-1382G=
ENST00000563422.5:c.676G= ENSP00000457885.1:p.Ala226=
ENST00000563786.5:c.616G= ENSP00000455241.1:p.Ala206=
ENST00000564003.5:c.343G= ENSP00000454312.1:p.Ala115=
ENST00000566377.5:c.676G= ENSP00000455405.1:p.Ala226=
ENST00000566556.1:n.724G=
ENST00000567177.1:c.454G= ENSP00000457013.1:p.Ala152=
ENST00000569931.5:c.616G= ENSP00000455161.1:p.Ala206=
NM_001289155.1:c.676G= NP_001276084.1:p.Ala226=
NM_001289156.1:c.526G= NP_001276085.1:p.Ala176=
NM_001289157.1:c.493G= NP_001276086.1:p.Ala165=
NM_002435.2:c.676G= NP_002426.1:p.Ala226=
XM_011521592.1:c.664G= XP_011519894.1:p.Ala222=
XM_011521593.1:c.616G= XP_011519895.1:p.Ala206=
NM_001330372.1:c.616G= NP_001317301.1:p.Ala206=
XM_017022208.1:c.616G= XP_016877697.1:p.Ala206=
XM_017022209.2:c.526G= XP_016877698.1:p.Ala176=
NM_002435.3:c.676G= MANE Select NP_002426.1:p.Ala226=
NM_001289155.2:c.676G= NP_001276084.1:p.Ala226=
NM_001289156.2:c.526G= NP_001276085.1:p.Ala176=
NM_001289157.2:c.493G= NP_001276086.1:p.Ala165=
NM_001330372.2:c.616G= NP_001317301.1:p.Ala206=