Canonical Allele Identifier: CA2187901989

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896310_74896312delinsGCC , CM000677.2:g.74896310_74896312delinsGCC	GRCh38
NC_000015.9:g.75188651_75188653delinsGCC , CM000677.1:g.75188651_75188653delinsGCC	GRCh37
NC_000015.8:g.72975704_72975706delinsGCC	NCBI36
NG_008921.1:g.11242_11244delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.829_831delinsGCC MANE Select	ENSP00000318318.6:p.Ala277=
ENST00000323744.10:c.646_648delinsGCC	ENSP00000318192.6:p.Ala216=
ENST00000352410.8:c.829_831delinsGCC	ENSP00000318318.6:p.Ala277=
ENST00000535694.5:c.679_681delinsGCC	ENSP00000440447.1:p.Ala227=
ENST00000562606.5:c.769_771delinsGCC	ENSP00000457020.1:p.Ala257=
ENST00000562800.5:c.256-1229_256-1227delinsGCC	ENSP00000457619.1:n.256-1229_256-1227delinsGCC
ENST00000563422.5:c.829_831delinsGCC	ENSP00000457885.1:p.Ala277=
ENST00000563786.5:c.769_771delinsGCC	ENSP00000455241.1:p.Ala257=
ENST00000564003.5:c.496_498delinsGCC	ENSP00000454312.1:p.Ala166=
ENST00000566377.5:c.829_831delinsGCC	ENSP00000455405.1:p.Ala277=
ENST00000566556.1:n.877_879delinsGCC
ENST00000567177.1:c.607_609delinsGCC	ENSP00000457013.1:p.Ala203=
ENST00000569931.5:c.769_771delinsGCC	ENSP00000455161.1:p.Ala257=
NM_001289155.1:c.829_831delinsGCC	NP_001276084.1:p.Ala277=
NM_001289156.1:c.679_681delinsGCC	NP_001276085.1:p.Ala227=
NM_001289157.1:c.646_648delinsGCC	NP_001276086.1:p.Ala216=
NM_002435.2:c.829_831delinsGCC	NP_002426.1:p.Ala277=
XM_011521592.1:c.817_819delinsGCC	XP_011519894.1:p.Ala273=
XM_011521593.1:c.769_771delinsGCC	XP_011519895.1:p.Ala257=
NM_001330372.1:c.769_771delinsGCC	NP_001317301.1:p.Ala257=
XM_017022208.1:c.769_771delinsGCC	XP_016877697.1:p.Ala257=
XM_017022209.2:c.679_681delinsGCC	XP_016877698.1:p.Ala227=
NM_002435.3:c.829_831delinsGCC MANE Select	NP_002426.1:p.Ala277=
NM_001289155.2:c.829_831delinsGCC	NP_001276084.1:p.Ala277=
NM_001289156.2:c.679_681delinsGCC	NP_001276085.1:p.Ala227=
NM_001289157.2:c.646_648delinsGCC	NP_001276086.1:p.Ala216=
NM_001330372.2:c.769_771delinsGCC	NP_001317301.1:p.Ala257=