Canonical Allele Identifier: CA2187894831
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74890618_74890619delinsAC , CM000677.2:g.74890618_74890619delinsAC GRCh38
NC_000015.9:g.75182959_75182960delinsAC , CM000677.1:g.75182959_75182960delinsAC GRCh37
NC_000015.8:g.72970012_72970013delinsAC NCBI36
NG_008921.1:g.5550_5551delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000352410.9:c.108_109delinsAC MANE Select ENSP00000318318.6:p.Pro36=
ENST00000323744.10:c.108_109delinsAC ENSP00000318192.6:p.Pro36=
ENST00000352410.8:c.108_109delinsAC ENSP00000318318.6:p.Pro36=
ENST00000535694.5:c.-7+529_-7+530delinsAC ENSP00000440447.1:n.-7+529_-7+530delinsAC
ENST00000561470.5:c.*4_*5delinsAC ENSP00000454267.1:n.*4_*5delinsAC
ENST00000562606.5:c.48_49delinsAC ENSP00000457020.1:p.Pro16=
ENST00000562800.5:c.108_109delinsAC ENSP00000457619.1:p.Pro36=
ENST00000563422.5:c.108_109delinsAC ENSP00000457885.1:p.Pro36=
ENST00000563786.5:c.48_49delinsAC ENSP00000455241.1:p.Pro16=
ENST00000564003.5:c.-7+529_-7+530delinsAC ENSP00000454312.1:n.-7+529_-7+530delinsAC
ENST00000564633.5:c.48_49delinsAC ENSP00000455383.1:p.Pro16=
ENST00000565576.5:c.108_109delinsAC ENSP00000454619.1:p.Pro36=
ENST00000566377.5:c.108_109delinsAC ENSP00000455405.1:p.Pro36=
ENST00000567116.5:n.139_140delinsAC
ENST00000567132.5:c.108_109delinsAC ENSP00000455972.1:p.Pro36=
ENST00000567177.1:c.69_70delinsAC ENSP00000457013.1:p.Pro23=
ENST00000567570.5:c.48_49delinsAC ENSP00000455477.1:p.Pro16=
ENST00000568303.1:n.225_226delinsAC
ENST00000568828.5:c.108_109delinsAC ENSP00000455065.1:p.Pro36=
ENST00000568840.1:n.217_218delinsAC
ENST00000568907.5:c.108_109delinsAC ENSP00000457494.1:p.Pro36=
ENST00000569233.5:c.108_109delinsAC ENSP00000454622.1:p.Pro36=
ENST00000569931.5:c.48_49delinsAC ENSP00000455161.1:p.Pro16=
NM_001289155.1:c.108_109delinsAC NP_001276084.1:p.Pro36=
NM_001289156.1:c.-7+529_-7+530delinsAC NP_001276085.1:n.-7+529_-7+530delinsAC
NM_001289157.1:c.108_109delinsAC NP_001276086.1:p.Pro36=
NM_002435.2:c.108_109delinsAC NP_002426.1:p.Pro36=
XM_011521592.1:c.96_97delinsAC XP_011519894.1:p.Pro32=
XM_011521593.1:c.48_49delinsAC XP_011519895.1:p.Pro16=
NM_001330372.1:c.48_49delinsAC NP_001317301.1:p.Pro16=
XM_017022208.1:c.48_49delinsAC XP_016877697.1:p.Pro16=
XM_017022209.2:c.-7+529_-7+530delinsAC XP_016877698.1:n.-7+529_-7+530delinsAC
NM_002435.3:c.108_109delinsAC MANE Select NP_002426.1:p.Pro36=
NM_001289155.2:c.108_109delinsAC NP_001276084.1:p.Pro36=
NM_001289156.2:c.-7+529_-7+530delinsAC NP_001276085.1:n.-7+529_-7+530delinsAC
NM_001289157.2:c.108_109delinsAC NP_001276086.1:p.Pro36=
NM_001330372.2:c.48_49delinsAC NP_001317301.1:p.Pro16=