Canonical Allele Identifier: CA2187902621

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896970G= , CM000677.2:g.74896970G=	GRCh38
NC_000015.9:g.75189311G= , CM000677.1:g.75189311G=	GRCh37
NC_000015.8:g.72976364G=	NCBI36
NG_008921.1:g.11902G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.845-41G= MANE Select	ENSP00000318318.6:n.845-41G=
ENST00000323744.10:c.662-41G=	ENSP00000318192.6:n.662-41G=
ENST00000352410.8:c.845-41G=	ENSP00000318318.6:n.845-41G=
ENST00000535694.5:c.695-41G=	ENSP00000440447.1:n.695-41G=
ENST00000562800.5:c.256-569G=	ENSP00000457619.1:n.256-569G=
ENST00000563786.5:c.785-41G=	ENSP00000455241.1:n.785-41G=
ENST00000566377.5:c.845-542G=	ENSP00000455405.1:n.845-542G=
ENST00000566556.1:n.1537G=
ENST00000567177.1:c.623-542G=	ENSP00000457013.1:n.623-542G=
ENST00000569931.5:c.785-41G=	ENSP00000455161.1:n.785-41G=
NM_001289155.1:c.845-542G=	NP_001276084.1:n.845-542G=
NM_001289156.1:c.695-41G=	NP_001276085.1:n.695-41G=
NM_001289157.1:c.662-41G=	NP_001276086.1:n.662-41G=
NM_002435.2:c.845-41G=	NP_002426.1:n.845-41G=
XM_011521592.1:c.833-41G=	XP_011519894.1:n.833-41G=
XM_011521593.1:c.785-41G=	XP_011519895.1:n.785-41G=
NM_001330372.1:c.785-41G=	NP_001317301.1:n.785-41G=
XM_017022208.1:c.785-542G=	XP_016877697.1:n.785-542G=
XM_017022209.2:c.695-542G=	XP_016877698.1:n.695-542G=
NM_002435.3:c.845-41G= MANE Select	NP_002426.1:n.845-41G=
NM_001289155.2:c.845-542G=	NP_001276084.1:n.845-542G=
NM_001289156.2:c.695-41G=	NP_001276085.1:n.695-41G=
NM_001289157.2:c.662-41G=	NP_001276086.1:n.662-41G=
NM_001330372.2:c.785-41G=	NP_001317301.1:n.785-41G=