Canonical Allele Identifier: CA2187901924

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896274G= , CM000677.2:g.74896274G=	GRCh38
NC_000015.9:g.75188615G= , CM000677.1:g.75188615G=	GRCh37
NC_000015.8:g.72975668G=	NCBI36
NG_008921.1:g.11206G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.793G= MANE Select	ENSP00000318318.6:p.Gly265=
ENST00000323744.10:c.610G=	ENSP00000318192.6:p.Gly204=
ENST00000352410.8:c.793G=	ENSP00000318318.6:p.Gly265=
ENST00000535694.5:c.643G=	ENSP00000440447.1:p.Gly215=
ENST00000562606.5:c.733G=	ENSP00000457020.1:p.Gly245=
ENST00000562800.5:c.256-1265G=	ENSP00000457619.1:n.256-1265G=
ENST00000563422.5:c.793G=	ENSP00000457885.1:p.Gly265=
ENST00000563786.5:c.733G=	ENSP00000455241.1:p.Gly245=
ENST00000564003.5:c.460G=	ENSP00000454312.1:p.Gly154=
ENST00000566377.5:c.793G=	ENSP00000455405.1:p.Gly265=
ENST00000566556.1:n.841G=
ENST00000567177.1:c.571G=	ENSP00000457013.1:p.Gly191=
ENST00000569931.5:c.733G=	ENSP00000455161.1:p.Gly245=
NM_001289155.1:c.793G=	NP_001276084.1:p.Gly265=
NM_001289156.1:c.643G=	NP_001276085.1:p.Gly215=
NM_001289157.1:c.610G=	NP_001276086.1:p.Gly204=
NM_002435.2:c.793G=	NP_002426.1:p.Gly265=
XM_011521592.1:c.781G=	XP_011519894.1:p.Gly261=
XM_011521593.1:c.733G=	XP_011519895.1:p.Gly245=
NM_001330372.1:c.733G=	NP_001317301.1:p.Gly245=
XM_017022208.1:c.733G=	XP_016877697.1:p.Gly245=
XM_017022209.2:c.643G=	XP_016877698.1:p.Gly215=
NM_002435.3:c.793G= MANE Select	NP_002426.1:p.Gly265=
NM_001289155.2:c.793G=	NP_001276084.1:p.Gly265=
NM_001289156.2:c.643G=	NP_001276085.1:p.Gly215=
NM_001289157.2:c.610G=	NP_001276086.1:p.Gly204=
NM_001330372.2:c.733G=	NP_001317301.1:p.Gly245=