Canonical Allele Identifier: CA272823541
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74893180C>T , CM000677.2:g.74893180C>T GRCh38
NC_000015.9:g.75185521C>T , CM000677.1:g.75185521C>T GRCh37
NC_000015.8:g.72972574C>T NCBI36
NG_008921.1:g.8112C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.530C>T MANE Select ENSP00000318318.6:p.Thr177Ile
ENST00000323744.10:c.487+378C>T ENSP00000318192.6:n.487+378C>T
ENST00000352410.8:c.530C>T ENSP00000318318.6:p.Thr177Ile
ENST00000535694.5:c.380C>T ENSP00000440447.1:p.Thr127Ile
ENST00000561470.5:c.*426C>T ENSP00000454267.1:n.*426C>T
ENST00000562606.5:c.470C>T ENSP00000457020.1:p.Thr157Ile
ENST00000562800.5:c.255+1691C>T ENSP00000457619.1:n.255+1691C>T
ENST00000563422.5:c.530C>T ENSP00000457885.1:p.Thr177Ile
ENST00000563786.5:c.470C>T ENSP00000455241.1:p.Thr157Ile
ENST00000564003.5:c.337+378C>T ENSP00000454312.1:n.337+378C>T
ENST00000564633.5:c.470C>T ENSP00000455383.1:p.Thr157Ile
ENST00000565576.5:c.530C>T ENSP00000454619.1:p.Thr177Ile
ENST00000566377.5:c.530C>T ENSP00000455405.1:p.Thr177Ile
ENST00000567132.5:c.488C>T ENSP00000455972.1:p.Thr163Ile
ENST00000567177.1:c.448+378C>T ENSP00000457013.1:n.448+378C>T
ENST00000568828.5:c.494C>T ENSP00000455065.1:p.Thr165Ile
ENST00000568907.5:c.440C>T ENSP00000457494.1:p.Thr147Ile
ENST00000569931.5:c.470C>T ENSP00000455161.1:p.Thr157Ile
NM_001289155.1:c.530C>T NP_001276084.1:p.Thr177Ile
NM_001289156.1:c.380C>T NP_001276085.1:p.Thr127Ile
NM_001289157.1:c.487+378C>T NP_001276086.1:n.487+378C>T
NM_002435.2:c.530C>T NP_002426.1:p.Thr177Ile
XM_011521592.1:c.518C>T XP_011519894.1:p.Thr173Ile
XM_011521593.1:c.470C>T XP_011519895.1:p.Thr157Ile
NM_001330372.1:c.470C>T NP_001317301.1:p.Thr157Ile
XM_017022208.1:c.470C>T XP_016877697.1:p.Thr157Ile
XM_017022209.2:c.380C>T XP_016877698.1:p.Thr127Ile
NM_002435.3:c.530C>T MANE Select NP_002426.1:p.Thr177Ile
NM_001289155.2:c.530C>T NP_001276084.1:p.Thr177Ile
NM_001289156.2:c.380C>T NP_001276085.1:p.Thr127Ile
NM_001289157.2:c.487+378C>T NP_001276086.1:n.487+378C>T
NM_001330372.2:c.470C>T NP_001317301.1:p.Thr157Ile