Canonical Allele Identifier: CA7662521
Gene: MPI HGNC NCBI

Linked Data

dbSNP Id: rs747198298

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74896160G>A , CM000677.2:g.74896160G>A GRCh38
NC_000015.9:g.75188501G>A , CM000677.1:g.75188501G>A GRCh37
NC_000015.8:g.72975554G>A NCBI36
NG_008921.1:g.11092G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.679G>A MANE Select ENSP00000318318.6:p.Gly227Arg
ENST00000323744.10:c.496G>A ENSP00000318192.6:p.Gly166Arg
ENST00000352410.8:c.679G>A ENSP00000318318.6:p.Gly227Arg
ENST00000535694.5:c.529G>A ENSP00000440447.1:p.Gly177Arg
ENST00000561470.5:c.*575G>A ENSP00000454267.1:n.*575G>A
ENST00000562606.5:c.619G>A ENSP00000457020.1:p.Gly207Arg
ENST00000562800.5:c.256-1379G>A ENSP00000457619.1:n.256-1379G>A
ENST00000563422.5:c.679G>A ENSP00000457885.1:p.Gly227Arg
ENST00000563786.5:c.619G>A ENSP00000455241.1:p.Gly207Arg
ENST00000564003.5:c.346G>A ENSP00000454312.1:p.Gly116Arg
ENST00000566377.5:c.679G>A ENSP00000455405.1:p.Gly227Arg
ENST00000566556.1:n.727G>A
ENST00000567177.1:c.457G>A ENSP00000457013.1:p.Gly153Arg
ENST00000569931.5:c.619G>A ENSP00000455161.1:p.Gly207Arg
NM_001289155.1:c.679G>A NP_001276084.1:p.Gly227Arg
NM_001289156.1:c.529G>A NP_001276085.1:p.Gly177Arg
NM_001289157.1:c.496G>A NP_001276086.1:p.Gly166Arg
NM_002435.2:c.679G>A NP_002426.1:p.Gly227Arg
XM_011521592.1:c.667G>A XP_011519894.1:p.Gly223Arg
XM_011521593.1:c.619G>A XP_011519895.1:p.Gly207Arg
NM_001330372.1:c.619G>A NP_001317301.1:p.Gly207Arg
XM_017022208.1:c.619G>A XP_016877697.1:p.Gly207Arg
XM_017022209.2:c.529G>A XP_016877698.1:p.Gly177Arg
NM_002435.3:c.679G>A MANE Select NP_002426.1:p.Gly227Arg
NM_001289155.2:c.679G>A NP_001276084.1:p.Gly227Arg
NM_001289156.2:c.529G>A NP_001276085.1:p.Gly177Arg
NM_001289157.2:c.496G>A NP_001276086.1:p.Gly166Arg
NM_001330372.2:c.619G>A NP_001317301.1:p.Gly207Arg