Canonical Allele Identifier: CA393176120
Gene: MPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74896322G>C , CM000677.2:g.74896322G>C GRCh38
NC_000015.9:g.75188663G>C , CM000677.1:g.75188663G>C GRCh37
NC_000015.8:g.72975716G>C NCBI36
NG_008921.1:g.11254G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.841G>C MANE Select ENSP00000318318.6:p.Gly281Arg
ENST00000323744.10:c.658G>C ENSP00000318192.6:p.Gly220Arg
ENST00000352410.8:c.841G>C ENSP00000318318.6:p.Gly281Arg
ENST00000535694.5:c.691G>C ENSP00000440447.1:p.Gly231Arg
ENST00000562606.5:c.781G>C ENSP00000457020.1:p.Gly261Arg
ENST00000562800.5:c.256-1217G>C ENSP00000457619.1:n.256-1217G>C
ENST00000563422.5:c.841G>C ENSP00000457885.1:p.Gly281Arg
ENST00000563786.5:c.781G>C ENSP00000455241.1:p.Gly261Arg
ENST00000564003.5:c.508G>C ENSP00000454312.1:p.Gly170Arg
ENST00000566377.5:c.841G>C ENSP00000455405.1:p.Gly281Arg
ENST00000566556.1:n.889G>C
ENST00000567177.1:c.619G>C ENSP00000457013.1:p.Gly207Arg
ENST00000569931.5:c.781G>C ENSP00000455161.1:p.Gly261Arg
NM_001289155.1:c.841G>C NP_001276084.1:p.Gly281Arg
NM_001289156.1:c.691G>C NP_001276085.1:p.Gly231Arg
NM_001289157.1:c.658G>C NP_001276086.1:p.Gly220Arg
NM_002435.2:c.841G>C NP_002426.1:p.Gly281Arg
XM_011521592.1:c.829G>C XP_011519894.1:p.Gly277Arg
XM_011521593.1:c.781G>C XP_011519895.1:p.Gly261Arg
NM_001330372.1:c.781G>C NP_001317301.1:p.Gly261Arg
XM_017022208.1:c.781G>C XP_016877697.1:p.Gly261Arg
XM_017022209.2:c.691G>C XP_016877698.1:p.Gly231Arg
NM_002435.3:c.841G>C MANE Select NP_002426.1:p.Gly281Arg
NM_001289155.2:c.841G>C NP_001276084.1:p.Gly281Arg
NM_001289156.2:c.691G>C NP_001276085.1:p.Gly231Arg
NM_001289157.2:c.658G>C NP_001276086.1:p.Gly220Arg
NM_001330372.2:c.781G>C NP_001317301.1:p.Gly261Arg