Canonical Allele Identifier: CA2575791675
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74892632A>G , CM000677.2:g.74892632A>G GRCh38
NC_000015.9:g.75184973A>G , CM000677.1:g.75184973A>G GRCh37
NC_000015.8:g.72972026A>G NCBI36
NG_008921.1:g.7564A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.346-29A>G MANE Select ENSP00000318318.6:n.346-29A>G
ENST00000323744.10:c.346-29A>G ENSP00000318192.6:n.346-29A>G
ENST00000352410.8:c.346-29A>G ENSP00000318318.6:n.346-29A>G
ENST00000535694.5:c.196-29A>G ENSP00000440447.1:n.196-29A>G
ENST00000561470.5:c.*242-29A>G ENSP00000454267.1:n.*242-29A>G
ENST00000562606.5:c.286-29A>G ENSP00000457020.1:n.286-29A>G
ENST00000562800.5:c.255+1143A>G ENSP00000457619.1:n.255+1143A>G
ENST00000563422.5:c.346-29A>G ENSP00000457885.1:n.346-29A>G
ENST00000563786.5:c.286-29A>G ENSP00000455241.1:n.286-29A>G
ENST00000564003.5:c.196-29A>G ENSP00000454312.1:n.196-29A>G
ENST00000564633.5:c.286-29A>G ENSP00000455383.1:n.286-29A>G
ENST00000565576.5:c.346-29A>G ENSP00000454619.1:n.346-29A>G
ENST00000566377.5:c.346-29A>G ENSP00000455405.1:n.346-29A>G
ENST00000567116.5:n.377-29A>G
ENST00000567132.5:c.331-56A>G ENSP00000455972.1:n.331-56A>G
ENST00000567177.1:c.307-29A>G ENSP00000457013.1:n.307-29A>G
ENST00000567570.5:c.286-29A>G ENSP00000455477.1:n.286-29A>G
ENST00000568828.5:c.310-29A>G ENSP00000455065.1:n.310-29A>G
ENST00000568840.1:n.455-29A>G
ENST00000568907.5:c.256-29A>G ENSP00000457494.1:n.256-29A>G
ENST00000569233.5:c.403-29A>G ENSP00000454622.1:n.403-29A>G
ENST00000569931.5:c.286-29A>G ENSP00000455161.1:n.286-29A>G
NM_001289155.1:c.346-29A>G NP_001276084.1:n.346-29A>G
NM_001289156.1:c.196-29A>G NP_001276085.1:n.196-29A>G
NM_001289157.1:c.346-29A>G NP_001276086.1:n.346-29A>G
NM_002435.2:c.346-29A>G NP_002426.1:n.346-29A>G
XM_011521592.1:c.334-29A>G XP_011519894.1:n.334-29A>G
XM_011521593.1:c.286-29A>G XP_011519895.1:n.286-29A>G
NM_001330372.1:c.286-29A>G NP_001317301.1:n.286-29A>G
XM_017022208.1:c.286-29A>G XP_016877697.1:n.286-29A>G
XM_017022209.2:c.196-29A>G XP_016877698.1:n.196-29A>G
NM_002435.3:c.346-29A>G MANE Select NP_002426.1:n.346-29A>G
NM_001289155.2:c.346-29A>G NP_001276084.1:n.346-29A>G
NM_001289156.2:c.196-29A>G NP_001276085.1:n.196-29A>G
NM_001289157.2:c.346-29A>G NP_001276086.1:n.346-29A>G
NM_001330372.2:c.286-29A>G NP_001317301.1:n.286-29A>G