Canonical Allele Identifier: CA393174465
Gene: MPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74893209T>C , CM000677.2:g.74893209T>C GRCh38
NC_000015.9:g.75185550T>C , CM000677.1:g.75185550T>C GRCh37
NC_000015.8:g.72972603T>C NCBI36
NG_008921.1:g.8141T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.559T>C MANE Select ENSP00000318318.6:p.Ser187Pro
ENST00000323744.10:c.487+407T>C ENSP00000318192.6:n.487+407T>C
ENST00000352410.8:c.559T>C ENSP00000318318.6:p.Ser187Pro
ENST00000535694.5:c.409T>C ENSP00000440447.1:p.Ser137Pro
ENST00000561470.5:c.*455T>C ENSP00000454267.1:n.*455T>C
ENST00000562606.5:c.499T>C ENSP00000457020.1:p.Ser167Pro
ENST00000562800.5:c.255+1720T>C ENSP00000457619.1:n.255+1720T>C
ENST00000563422.5:c.559T>C ENSP00000457885.1:p.Ser187Pro
ENST00000563786.5:c.499T>C ENSP00000455241.1:p.Ser167Pro
ENST00000564003.5:c.337+407T>C ENSP00000454312.1:n.337+407T>C
ENST00000564633.5:c.499T>C ENSP00000455383.1:p.Ser167Pro
ENST00000565576.5:c.559T>C ENSP00000454619.1:p.Ser187Pro
ENST00000566377.5:c.559T>C ENSP00000455405.1:p.Ser187Pro
ENST00000567132.5:c.517T>C ENSP00000455972.1:p.Ser173Pro
ENST00000567177.1:c.448+407T>C ENSP00000457013.1:n.448+407T>C
ENST00000568828.5:c.523T>C ENSP00000455065.1:p.Ser175Pro
ENST00000568907.5:c.469T>C ENSP00000457494.1:p.Ser157Pro
ENST00000569931.5:c.499T>C ENSP00000455161.1:p.Ser167Pro
NM_001289155.1:c.559T>C NP_001276084.1:p.Ser187Pro
NM_001289156.1:c.409T>C NP_001276085.1:p.Ser137Pro
NM_001289157.1:c.487+407T>C NP_001276086.1:n.487+407T>C
NM_002435.2:c.559T>C NP_002426.1:p.Ser187Pro
XM_011521592.1:c.547T>C XP_011519894.1:p.Ser183Pro
XM_011521593.1:c.499T>C XP_011519895.1:p.Ser167Pro
NM_001330372.1:c.499T>C NP_001317301.1:p.Ser167Pro
XM_017022208.1:c.499T>C XP_016877697.1:p.Ser167Pro
XM_017022209.2:c.409T>C XP_016877698.1:p.Ser137Pro
NM_002435.3:c.559T>C MANE Select NP_002426.1:p.Ser187Pro
NM_001289155.2:c.559T>C NP_001276084.1:p.Ser187Pro
NM_001289156.2:c.409T>C NP_001276085.1:p.Ser137Pro
NM_001289157.2:c.487+407T>C NP_001276086.1:n.487+407T>C
NM_001330372.2:c.499T>C NP_001317301.1:p.Ser167Pro