Canonical Allele Identifier: CA715703774
Gene: MPI HGNC NCBI

Linked Data

dbSNP Id: rs1266197265

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74892646del , CM000677.2:g.74892646del GRCh38
NC_000015.9:g.75184987del , CM000677.1:g.75184987del GRCh37
NC_000015.8:g.72972040del NCBI36
NG_008921.1:g.7578del

Transcript Alleles

HGVS Amino-acid change
ENST00000352410.9:c.346-15del MANE Select ENSP00000318318.6:n.346-15del
ENST00000323744.10:c.346-15del ENSP00000318192.6:n.346-15del
ENST00000352410.8:c.346-15del ENSP00000318318.6:n.346-15del
ENST00000535694.5:c.196-15del ENSP00000440447.1:n.196-15del
ENST00000561470.5:c.*242-15del ENSP00000454267.1:n.*242-15del
ENST00000562606.5:c.286-15del ENSP00000457020.1:n.286-15del
ENST00000562800.5:c.255+1157del ENSP00000457619.1:n.255+1157del
ENST00000563422.5:c.346-15del ENSP00000457885.1:n.346-15del
ENST00000563786.5:c.286-15del ENSP00000455241.1:n.286-15del
ENST00000564003.5:c.196-15del ENSP00000454312.1:n.196-15del
ENST00000564633.5:c.286-15del ENSP00000455383.1:n.286-15del
ENST00000565576.5:c.346-15del ENSP00000454619.1:n.346-15del
ENST00000566377.5:c.346-15del ENSP00000455405.1:n.346-15del
ENST00000567116.5:n.377-15del
ENST00000567132.5:c.331-42del ENSP00000455972.1:n.331-42del
ENST00000567177.1:c.307-15del ENSP00000457013.1:n.307-15del
ENST00000567570.5:c.286-15del ENSP00000455477.1:n.286-15del
ENST00000568828.5:c.310-15del ENSP00000455065.1:n.310-15del
ENST00000568840.1:n.455-15del
ENST00000568907.5:c.256-15del ENSP00000457494.1:n.256-15del
ENST00000569233.5:c.403-15del ENSP00000454622.1:n.403-15del
ENST00000569931.5:c.286-15del ENSP00000455161.1:n.286-15del
NM_001289155.1:c.346-15del NP_001276084.1:n.346-15del
NM_001289156.1:c.196-15del NP_001276085.1:n.196-15del
NM_001289157.1:c.346-15del NP_001276086.1:n.346-15del
NM_002435.2:c.346-15del NP_002426.1:n.346-15del
XM_011521592.1:c.334-15del XP_011519894.1:n.334-15del
XM_011521593.1:c.286-15del XP_011519895.1:n.286-15del
NM_001330372.1:c.286-15del NP_001317301.1:n.286-15del
XM_017022208.1:c.286-15del XP_016877697.1:n.286-15del
XM_017022209.2:c.196-15del XP_016877698.1:n.196-15del
NM_002435.3:c.346-15del MANE Select NP_002426.1:n.346-15del
NM_001289155.2:c.346-15del NP_001276084.1:n.346-15del
NM_001289156.2:c.196-15del NP_001276085.1:n.196-15del
NM_001289157.2:c.346-15del NP_001276086.1:n.346-15del
NM_001330372.2:c.286-15del NP_001317301.1:n.286-15del