Canonical Allele Identifier: CA2187901871

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896250C= , CM000677.2:g.74896250C=	GRCh38
NC_000015.9:g.75188591C= , CM000677.1:g.75188591C=	GRCh37
NC_000015.8:g.72975644C=	NCBI36
NG_008921.1:g.11182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.769C= MANE Select	ENSP00000318318.6:p.Leu257=
ENST00000323744.10:c.586C=	ENSP00000318192.6:p.Leu196=
ENST00000352410.8:c.769C=	ENSP00000318318.6:p.Leu257=
ENST00000535694.5:c.619C=	ENSP00000440447.1:p.Leu207=
ENST00000562606.5:c.709C=	ENSP00000457020.1:p.Leu237=
ENST00000562800.5:c.256-1289C=	ENSP00000457619.1:n.256-1289C=
ENST00000563422.5:c.769C=	ENSP00000457885.1:p.Leu257=
ENST00000563786.5:c.709C=	ENSP00000455241.1:p.Leu237=
ENST00000564003.5:c.436C=	ENSP00000454312.1:p.Leu146=
ENST00000566377.5:c.769C=	ENSP00000455405.1:p.Leu257=
ENST00000566556.1:n.817C=
ENST00000567177.1:c.547C=	ENSP00000457013.1:p.Leu183=
ENST00000569931.5:c.709C=	ENSP00000455161.1:p.Leu237=
NM_001289155.1:c.769C=	NP_001276084.1:p.Leu257=
NM_001289156.1:c.619C=	NP_001276085.1:p.Leu207=
NM_001289157.1:c.586C=	NP_001276086.1:p.Leu196=
NM_002435.2:c.769C=	NP_002426.1:p.Leu257=
XM_011521592.1:c.757C=	XP_011519894.1:p.Leu253=
XM_011521593.1:c.709C=	XP_011519895.1:p.Leu237=
NM_001330372.1:c.709C=	NP_001317301.1:p.Leu237=
XM_017022208.1:c.709C=	XP_016877697.1:p.Leu237=
XM_017022209.2:c.619C=	XP_016877698.1:p.Leu207=
NM_002435.3:c.769C= MANE Select	NP_002426.1:p.Leu257=
NM_001289155.2:c.769C=	NP_001276084.1:p.Leu257=
NM_001289156.2:c.619C=	NP_001276085.1:p.Leu207=
NM_001289157.2:c.586C=	NP_001276086.1:p.Leu196=
NM_001330372.2:c.709C=	NP_001317301.1:p.Leu237=