Canonical Allele Identifier: CA2629529443
Gene: MPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74892732dup , CM000677.2:g.74892732dup GRCh38
NC_000015.9:g.75185073dup , CM000677.1:g.75185073dup GRCh37
NC_000015.8:g.72972126dup NCBI36
NG_008921.1:g.7664dup

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.417dup MANE Select ENSP00000318318.6:p.Ile140HisfsTer16
ENST00000323744.10:c.417dup ENSP00000318192.6:p.Ile140HisfsTer16
ENST00000352410.8:c.417dup ENSP00000318318.6:p.Ile140HisfsTer16
ENST00000535694.5:c.267dup ENSP00000440447.1:p.Ile90HisfsTer16
ENST00000561470.5:c.*313dup ENSP00000454267.1:n.*313dup
ENST00000562606.5:c.357dup ENSP00000457020.1:p.Ile120HisfsTer16
ENST00000562800.5:c.255+1243dup ENSP00000457619.1:n.255+1243dup
ENST00000563422.5:c.417dup ENSP00000457885.1:p.Ile140HisfsTer16
ENST00000563786.5:c.357dup ENSP00000455241.1:p.Ile120HisfsTer16
ENST00000564003.5:c.267dup ENSP00000454312.1:p.Ile90HisfsTer16
ENST00000564633.5:c.357dup ENSP00000455383.1:p.Ile120HisfsTer16
ENST00000565576.5:c.417dup ENSP00000454619.1:p.Ile140HisfsTer16
ENST00000566377.5:c.417dup ENSP00000455405.1:p.Ile140HisfsTer16
ENST00000567116.5:n.448dup
ENST00000567132.5:c.375dup ENSP00000455972.1:p.Ile126HisfsTer16
ENST00000567177.1:c.378dup ENSP00000457013.1:p.Ile127HisfsTer16
ENST00000567570.5:c.357dup
ENST00000568828.5:c.381dup ENSP00000455065.1:p.Ile128HisfsTer16
ENST00000568840.1:n.526dup
ENST00000568907.5:c.327dup ENSP00000457494.1:p.Ile110HisfsTer16
ENST00000569233.5:c.474dup ENSP00000454622.1:p.Ile159HisfsTer16
ENST00000569931.5:c.357dup ENSP00000455161.1:p.Ile120HisfsTer16
NM_001289155.1:c.417dup NP_001276084.1:p.Ile140HisfsTer16
NM_001289156.1:c.267dup NP_001276085.1:p.Ile90HisfsTer16
NM_001289157.1:c.417dup NP_001276086.1:p.Ile140HisfsTer16
NM_002435.2:c.417dup NP_002426.1:p.Ile140HisfsTer16
XM_011521592.1:c.405dup XP_011519894.1:p.Ile136HisfsTer16
XM_011521593.1:c.357dup XP_011519895.1:p.Ile120HisfsTer16
NM_001330372.1:c.357dup NP_001317301.1:p.Ile120HisfsTer16
XM_017022208.1:c.357dup XP_016877697.1:p.Ile120HisfsTer16
XM_017022209.2:c.267dup XP_016877698.1:p.Ile90HisfsTer16
NM_002435.3:c.417dup MANE Select NP_002426.1:p.Ile140HisfsTer16
NM_001289155.2:c.417dup NP_001276084.1:p.Ile140HisfsTer16
NM_001289156.2:c.267dup NP_001276085.1:p.Ile90HisfsTer16
NM_001289157.2:c.417dup NP_001276086.1:p.Ile140HisfsTer16
NM_001330372.2:c.357dup NP_001317301.1:p.Ile120HisfsTer16