Canonical Allele Identifier: CA2187901716

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896159C= , CM000677.2:g.74896159C=	GRCh38
NC_000015.9:g.75188500C= , CM000677.1:g.75188500C=	GRCh37
NC_000015.8:g.72975553C=	NCBI36
NG_008921.1:g.11091C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.678C= MANE Select	ENSP00000318318.6:p.Ala226=
ENST00000323744.10:c.495C=	ENSP00000318192.6:p.Ala165=
ENST00000352410.8:c.678C=	ENSP00000318318.6:p.Ala226=
ENST00000535694.5:c.528C=	ENSP00000440447.1:p.Ala176=
ENST00000561470.5:c.*574C=	ENSP00000454267.1:n.*574C=
ENST00000562606.5:c.618C=	ENSP00000457020.1:p.Ala206=
ENST00000562800.5:c.256-1380C=	ENSP00000457619.1:n.256-1380C=
ENST00000563422.5:c.678C=	ENSP00000457885.1:p.Ala226=
ENST00000563786.5:c.618C=	ENSP00000455241.1:p.Ala206=
ENST00000564003.5:c.345C=	ENSP00000454312.1:p.Ala115=
ENST00000566377.5:c.678C=	ENSP00000455405.1:p.Ala226=
ENST00000566556.1:n.726C=
ENST00000567177.1:c.456C=	ENSP00000457013.1:p.Ala152=
ENST00000569931.5:c.618C=	ENSP00000455161.1:p.Ala206=
NM_001289155.1:c.678C=	NP_001276084.1:p.Ala226=
NM_001289156.1:c.528C=	NP_001276085.1:p.Ala176=
NM_001289157.1:c.495C=	NP_001276086.1:p.Ala165=
NM_002435.2:c.678C=	NP_002426.1:p.Ala226=
XM_011521592.1:c.666C=	XP_011519894.1:p.Ala222=
XM_011521593.1:c.618C=	XP_011519895.1:p.Ala206=
NM_001330372.1:c.618C=	NP_001317301.1:p.Ala206=
XM_017022208.1:c.618C=	XP_016877697.1:p.Ala206=
XM_017022209.2:c.528C=	XP_016877698.1:p.Ala176=
NM_002435.3:c.678C= MANE Select	NP_002426.1:p.Ala226=
NM_001289155.2:c.678C=	NP_001276084.1:p.Ala226=
NM_001289156.2:c.528C=	NP_001276085.1:p.Ala176=
NM_001289157.2:c.495C=	NP_001276086.1:p.Ala165=
NM_001330372.2:c.618C=	NP_001317301.1:p.Ala206=