Canonical Allele Identifier: CA2187902031

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896342C= , CM000677.2:g.74896342C=	GRCh38
NC_000015.9:g.75188683C= , CM000677.1:g.75188683C=	GRCh37
NC_000015.8:g.72975736C=	NCBI36
NG_008921.1:g.11274C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.844+17C= MANE Select	ENSP00000318318.6:n.844+17C=
ENST00000323744.10:c.661+17C=	ENSP00000318192.6:n.661+17C=
ENST00000352410.8:c.844+17C=	ENSP00000318318.6:n.844+17C=
ENST00000535694.5:c.694+17C=	ENSP00000440447.1:n.694+17C=
ENST00000562606.5:c.801C=	ENSP00000457020.1:p.Ser267=
ENST00000562800.5:c.256-1197C=	ENSP00000457619.1:n.256-1197C=
ENST00000563422.5:c.861C=	ENSP00000457885.1:p.Ser287=
ENST00000563786.5:c.784+17C=	ENSP00000455241.1:n.784+17C=
ENST00000564003.5:c.528C=	ENSP00000454312.1:p.Ser176=
ENST00000566377.5:c.844+17C=	ENSP00000455405.1:n.844+17C=
ENST00000566556.1:n.909C=
ENST00000567177.1:c.622+17C=	ENSP00000457013.1:n.622+17C=
ENST00000569931.5:c.784+17C=	ENSP00000455161.1:n.784+17C=
NM_001289155.1:c.844+17C=	NP_001276084.1:n.844+17C=
NM_001289156.1:c.694+17C=	NP_001276085.1:n.694+17C=
NM_001289157.1:c.661+17C=	NP_001276086.1:n.661+17C=
NM_002435.2:c.844+17C=	NP_002426.1:n.844+17C=
XM_011521592.1:c.832+17C=	XP_011519894.1:n.832+17C=
XM_011521593.1:c.784+17C=	XP_011519895.1:n.784+17C=
NM_001330372.1:c.784+17C=	NP_001317301.1:n.784+17C=
XM_017022208.1:c.784+17C=	XP_016877697.1:n.784+17C=
XM_017022209.2:c.694+17C=	XP_016877698.1:n.694+17C=
NM_002435.3:c.844+17C= MANE Select	NP_002426.1:n.844+17C=
NM_001289155.2:c.844+17C=	NP_001276084.1:n.844+17C=
NM_001289156.2:c.694+17C=	NP_001276085.1:n.694+17C=
NM_001289157.2:c.661+17C=	NP_001276086.1:n.661+17C=
NM_001330372.2:c.784+17C=	NP_001317301.1:n.784+17C=