Canonical Allele Identifier: CA2187902051

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896366C= , CM000677.2:g.74896366C=	GRCh38
NC_000015.9:g.75188707C= , CM000677.1:g.75188707C=	GRCh37
NC_000015.8:g.72975760C=	NCBI36
NG_008921.1:g.11298C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.844+41C= MANE Select	ENSP00000318318.6:n.844+41C=
ENST00000323744.10:c.661+41C=	ENSP00000318192.6:n.661+41C=
ENST00000352410.8:c.844+41C=	ENSP00000318318.6:n.844+41C=
ENST00000535694.5:c.694+41C=	ENSP00000440447.1:n.694+41C=
ENST00000562606.5:c.825C=	ENSP00000457020.1:p.Cys275=
ENST00000562800.5:c.256-1173C=	ENSP00000457619.1:n.256-1173C=
ENST00000563422.5:c.885C=	ENSP00000457885.1:p.Cys295=
ENST00000563786.5:c.784+41C=	ENSP00000455241.1:n.784+41C=
ENST00000564003.5:c.552C=	ENSP00000454312.1:p.Cys184=
ENST00000566377.5:c.844+41C=	ENSP00000455405.1:n.844+41C=
ENST00000566556.1:n.933C=
ENST00000567177.1:c.622+41C=	ENSP00000457013.1:n.622+41C=
ENST00000569931.5:c.784+41C=	ENSP00000455161.1:n.784+41C=
NM_001289155.1:c.844+41C=	NP_001276084.1:n.844+41C=
NM_001289156.1:c.694+41C=	NP_001276085.1:n.694+41C=
NM_001289157.1:c.661+41C=	NP_001276086.1:n.661+41C=
NM_002435.2:c.844+41C=	NP_002426.1:n.844+41C=
XM_011521592.1:c.832+41C=	XP_011519894.1:n.832+41C=
XM_011521593.1:c.784+41C=	XP_011519895.1:n.784+41C=
NM_001330372.1:c.784+41C=	NP_001317301.1:n.784+41C=
XM_017022208.1:c.784+41C=	XP_016877697.1:n.784+41C=
XM_017022209.2:c.694+41C=	XP_016877698.1:n.694+41C=
NM_002435.3:c.844+41C= MANE Select	NP_002426.1:n.844+41C=
NM_001289155.2:c.844+41C=	NP_001276084.1:n.844+41C=
NM_001289156.2:c.694+41C=	NP_001276085.1:n.694+41C=
NM_001289157.2:c.661+41C=	NP_001276086.1:n.661+41C=
NM_001330372.2:c.784+41C=	NP_001317301.1:n.784+41C=