Canonical Allele Identifier: CA2187901815

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896226A= , CM000677.2:g.74896226A=	GRCh38
NC_000015.9:g.75188567A= , CM000677.1:g.75188567A=	GRCh37
NC_000015.8:g.72975620A=	NCBI36
NG_008921.1:g.11158A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.745A= MANE Select	ENSP00000318318.6:p.Ile249=
ENST00000323744.10:c.562A=	ENSP00000318192.6:p.Ile188=
ENST00000352410.8:c.745A=	ENSP00000318318.6:p.Ile249=
ENST00000535694.5:c.595A=	ENSP00000440447.1:p.Ile199=
ENST00000562606.5:c.685A=	ENSP00000457020.1:p.Ile229=
ENST00000562800.5:c.256-1313A=	ENSP00000457619.1:n.256-1313A=
ENST00000563422.5:c.745A=	ENSP00000457885.1:p.Ile249=
ENST00000563786.5:c.685A=	ENSP00000455241.1:p.Ile229=
ENST00000564003.5:c.412A=	ENSP00000454312.1:p.Ile138=
ENST00000566377.5:c.745A=	ENSP00000455405.1:p.Ile249=
ENST00000566556.1:n.793A=
ENST00000567177.1:c.523A=	ENSP00000457013.1:p.Ile175=
ENST00000569931.5:c.685A=	ENSP00000455161.1:p.Ile229=
NM_001289155.1:c.745A=	NP_001276084.1:p.Ile249=
NM_001289156.1:c.595A=	NP_001276085.1:p.Ile199=
NM_001289157.1:c.562A=	NP_001276086.1:p.Ile188=
NM_002435.2:c.745A=	NP_002426.1:p.Ile249=
XM_011521592.1:c.733A=	XP_011519894.1:p.Ile245=
XM_011521593.1:c.685A=	XP_011519895.1:p.Ile229=
NM_001330372.1:c.685A=	NP_001317301.1:p.Ile229=
XM_017022208.1:c.685A=	XP_016877697.1:p.Ile229=
XM_017022209.2:c.595A=	XP_016877698.1:p.Ile199=
NM_002435.3:c.745A= MANE Select	NP_002426.1:p.Ile249=
NM_001289155.2:c.745A=	NP_001276084.1:p.Ile249=
NM_001289156.2:c.595A=	NP_001276085.1:p.Ile199=
NM_001289157.2:c.562A=	NP_001276086.1:p.Ile188=
NM_001330372.2:c.685A=	NP_001317301.1:p.Ile229=