Canonical Allele Identifier: CA2187902623

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896972A= , CM000677.2:g.74896972A=	GRCh38
NC_000015.9:g.75189313A= , CM000677.1:g.75189313A=	GRCh37
NC_000015.8:g.72976366A=	NCBI36
NG_008921.1:g.11904A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.845-39A= MANE Select	ENSP00000318318.6:n.845-39A=
ENST00000323744.10:c.662-39A=	ENSP00000318192.6:n.662-39A=
ENST00000352410.8:c.845-39A=	ENSP00000318318.6:n.845-39A=
ENST00000535694.5:c.695-39A=	ENSP00000440447.1:n.695-39A=
ENST00000562800.5:c.256-567A=	ENSP00000457619.1:n.256-567A=
ENST00000563786.5:c.785-39A=	ENSP00000455241.1:n.785-39A=
ENST00000566377.5:c.845-540A=	ENSP00000455405.1:n.845-540A=
ENST00000566556.1:n.1539A=
ENST00000567177.1:c.623-540A=	ENSP00000457013.1:n.623-540A=
ENST00000569931.5:c.785-39A=	ENSP00000455161.1:n.785-39A=
NM_001289155.1:c.845-540A=	NP_001276084.1:n.845-540A=
NM_001289156.1:c.695-39A=	NP_001276085.1:n.695-39A=
NM_001289157.1:c.662-39A=	NP_001276086.1:n.662-39A=
NM_002435.2:c.845-39A=	NP_002426.1:n.845-39A=
XM_011521592.1:c.833-39A=	XP_011519894.1:n.833-39A=
XM_011521593.1:c.785-39A=	XP_011519895.1:n.785-39A=
NM_001330372.1:c.785-39A=	NP_001317301.1:n.785-39A=
XM_017022208.1:c.785-540A=	XP_016877697.1:n.785-540A=
XM_017022209.2:c.695-540A=	XP_016877698.1:n.695-540A=
NM_002435.3:c.845-39A= MANE Select	NP_002426.1:n.845-39A=
NM_001289155.2:c.845-540A=	NP_001276084.1:n.845-540A=
NM_001289156.2:c.695-39A=	NP_001276085.1:n.695-39A=
NM_001289157.2:c.662-39A=	NP_001276086.1:n.662-39A=
NM_001330372.2:c.785-39A=	NP_001317301.1:n.785-39A=