Canonical Allele Identifier: CA2187894218

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74890166_74890175delinsGGTTGAGTCC , CM000677.2:g.74890166_74890175delinsGGTTGAGTCC	GRCh38
NC_000015.9:g.75182507_75182516delinsGGTTGAGTCC , CM000677.1:g.75182507_75182516delinsGGTTGAGTCC	GRCh37
NC_000015.8:g.72969560_72969569delinsGGTTGAGTCC	NCBI36
NG_008921.1:g.5098_5107delinsGGTTGAGTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.16+77_16+86delinsGGTTGAGTCC MANE Select	ENSP00000318318.6:n.16+77_16+86delinsGGTTGAGTCC
ENST00000323744.10:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000318192.6:n.16+77_16+86delinsGGTTGAGTCC
ENST00000352410.8:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000318318.6:n.16+77_16+86delinsGGTTGAGTCC
ENST00000535694.5:c.-7+77_-7+86delinsGGTTGAGTCC	ENSP00000440447.1:n.-7+77_-7+86delinsGGTTGAGTCC
ENST00000561470.5:c.93_102delinsGGTTGAGTCC	ENSP00000454267.1:p.Gln31=
ENST00000562606.5:c.-19+77_-19+86delinsGGTTGAGTCC	ENSP00000457020.1:n.-19+77_-19+86delinsGGTTGAGTCC
ENST00000562800.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000457619.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000563422.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000457885.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000563786.5:c.-134+77_-134+86delinsGGTTGAGTCC	ENSP00000455241.1:n.-134+77_-134+86delinsGGTTGAGTCC
ENST00000564003.5:c.-7+77_-7+86delinsGGTTGAGTCC	ENSP00000454312.1:n.-7+77_-7+86delinsGGTTGAGTCC
ENST00000564633.5:c.-16+77_-16+86delinsGGTTGAGTCC	ENSP00000455383.1:n.-16+77_-16+86delinsGGTTGAGTCC
ENST00000565576.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000454619.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000566377.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000455405.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000567116.5:n.47+77_47+86delinsGGTTGAGTCC
ENST00000567132.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000455972.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000567570.5:c.-405_-396delinsGGTTGAGTCC	ENSP00000455477.1:n.-405_-396delinsGGTTGAGTCC
ENST00000568303.1:n.44+77_44+86delinsGGTTGAGTCC
ENST00000568828.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000455065.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000568840.1:n.90_99delinsGGTTGAGTCC
ENST00000568907.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000457494.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000569233.5:c.16+77_16+86delinsGGTTGAGTCC	ENSP00000454622.1:n.16+77_16+86delinsGGTTGAGTCC
ENST00000569931.5:c.-19+77_-19+86delinsGGTTGAGTCC	ENSP00000455161.1:n.-19+77_-19+86delinsGGTTGAGTCC
NM_001289155.1:c.16+77_16+86delinsGGTTGAGTCC	NP_001276084.1:n.16+77_16+86delinsGGTTGAGTCC
NM_001289156.1:c.-7+77_-7+86delinsGGTTGAGTCC	NP_001276085.1:n.-7+77_-7+86delinsGGTTGAGTCC
NM_001289157.1:c.16+77_16+86delinsGGTTGAGTCC	NP_001276086.1:n.16+77_16+86delinsGGTTGAGTCC
NM_002435.2:c.16+77_16+86delinsGGTTGAGTCC	NP_002426.1:n.16+77_16+86delinsGGTTGAGTCC
XM_011521592.1:c.-32_-23delinsGGTTGAGTCC	XP_011519894.1:n.-32_-23delinsGGTTGAGTCC
XM_011521593.1:c.-134+77_-134+86delinsGGTTGAGTCC	XP_011519895.1:n.-134+77_-134+86delinsGGTTGAGTCC
NM_001330372.1:c.-134+77_-134+86delinsGGTTGAGTCC	NP_001317301.1:n.-134+77_-134+86delinsGGTTGAGTCC
XM_017022208.1:c.-134+77_-134+86delinsGGTTGAGTCC	XP_016877697.1:n.-134+77_-134+86delinsGGTTGAGTCC
XM_017022209.2:c.-7+77_-7+86delinsGGTTGAGTCC	XP_016877698.1:n.-7+77_-7+86delinsGGTTGAGTCC
NM_002435.3:c.16+77_16+86delinsGGTTGAGTCC MANE Select	NP_002426.1:n.16+77_16+86delinsGGTTGAGTCC
NM_001289155.2:c.16+77_16+86delinsGGTTGAGTCC	NP_001276084.1:n.16+77_16+86delinsGGTTGAGTCC
NM_001289156.2:c.-7+77_-7+86delinsGGTTGAGTCC	NP_001276085.1:n.-7+77_-7+86delinsGGTTGAGTCC
NM_001289157.2:c.16+77_16+86delinsGGTTGAGTCC	NP_001276086.1:n.16+77_16+86delinsGGTTGAGTCC
NM_001330372.2:c.-134+77_-134+86delinsGGTTGAGTCC	NP_001317301.1:n.-134+77_-134+86delinsGGTTGAGTCC