Canonical Allele Identifier: CA2499223094
Gene: MPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74893328_74893329delinsTG , CM000677.2:g.74893328_74893329delinsTG GRCh38
NC_000015.9:g.75185669_75185670delinsTG , CM000677.1:g.75185669_75185670delinsTG GRCh37
NC_000015.8:g.72972722_72972723delinsTG NCBI36
NG_008921.1:g.8260_8261delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_002435.3:c.670+8_670+9delinsTG MANE Select NP_002426.1:n.670+8_670+9delinsTG
ENST00000352410.9:c.670+8_670+9delinsTG MANE Select ENSP00000318318.6:n.670+8_670+9delinsTG
NM_001289155.1:c.670+8_670+9delinsTG NP_001276084.1:n.670+8_670+9delinsTG
NM_001289155.2:c.670+8_670+9delinsTG NP_001276084.1:n.670+8_670+9delinsTG
NM_001289156.1:c.520+8_520+9delinsTG NP_001276085.1:n.520+8_520+9delinsTG
NM_001289156.2:c.520+8_520+9delinsTG NP_001276085.1:n.520+8_520+9delinsTG
NM_001289157.1:c.487+526_487+527delinsTG NP_001276086.1:n.487+526_487+527delinsTG
NM_001289157.2:c.487+526_487+527delinsTG NP_001276086.1:n.487+526_487+527delinsTG
NM_001330372.1:c.610+8_610+9delinsTG NP_001317301.1:n.610+8_610+9delinsTG
NM_001330372.2:c.610+8_610+9delinsTG NP_001317301.1:n.610+8_610+9delinsTG
NM_002435.2:c.670+8_670+9delinsTG NP_002426.1:n.670+8_670+9delinsTG
ENST00000323744.10:c.487+526_487+527delinsTG ENSP00000318192.6:n.487+526_487+527delinsTG
ENST00000352410.8:c.670+8_670+9delinsTG ENSP00000318318.6:n.670+8_670+9delinsTG
ENST00000535694.5:c.520+8_520+9delinsTG ENSP00000440447.1:n.520+8_520+9delinsTG
ENST00000561470.5:c.*566+8_*566+9delinsTG ENSP00000454267.1:n.*566+8_*566+9delinsTG
ENST00000562606.5:c.610+8_610+9delinsTG ENSP00000457020.1:n.610+8_610+9delinsTG
ENST00000562800.5:c.255+1839_255+1840delinsTG ENSP00000457619.1:n.255+1839_255+1840delinsTG
ENST00000563422.5:c.670+8_670+9delinsTG ENSP00000457885.1:n.670+8_670+9delinsTG
ENST00000563786.5:c.610+8_610+9delinsTG ENSP00000455241.1:n.610+8_610+9delinsTG
ENST00000564003.5:c.337+526_337+527delinsTG ENSP00000454312.1:n.337+526_337+527delinsTG
ENST00000565576.5:c.678_679delinsTG ENSP00000454619.1:p.Ser227Gly
ENST00000566377.5:c.670+8_670+9delinsTG ENSP00000455405.1:n.670+8_670+9delinsTG
ENST00000567177.1:c.448+526_448+527delinsTG ENSP00000457013.1:n.448+526_448+527delinsTG
ENST00000569931.5:c.610+8_610+9delinsTG ENSP00000455161.1:n.610+8_610+9delinsTG
XM_011521592.1:c.658+8_658+9delinsTG XP_011519894.1:n.658+8_658+9delinsTG
XM_011521593.1:c.610+8_610+9delinsTG XP_011519895.1:n.610+8_610+9delinsTG
XM_017022208.1:c.610+8_610+9delinsTG XP_016877697.1:n.610+8_610+9delinsTG
XM_017022209.2:c.520+8_520+9delinsTG XP_016877698.1:n.520+8_520+9delinsTG