Canonical Allele Identifier: CA2187902758

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74897064C= , CM000677.2:g.74897064C=	GRCh38
NC_000015.9:g.75189405C= , CM000677.1:g.75189405C=	GRCh37
NC_000015.8:g.72976458C=	NCBI36
NG_008921.1:g.11996C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.898C= MANE Select	ENSP00000318318.6:p.Pro300=
ENST00000323744.10:c.715C=	ENSP00000318192.6:p.Pro239=
ENST00000352410.8:c.898C=	ENSP00000318318.6:p.Pro300=
ENST00000535694.5:c.748C=	ENSP00000440447.1:p.Pro250=
ENST00000562800.5:c.256-475C=	ENSP00000457619.1:n.256-475C=
ENST00000563786.5:c.838C=	ENSP00000455241.1:p.Pro280=
ENST00000566377.5:c.845-448C=	ENSP00000455405.1:n.845-448C=
ENST00000566556.1:n.1631C=
ENST00000567177.1:c.623-448C=	ENSP00000457013.1:n.623-448C=
ENST00000569931.5:c.838C=	ENSP00000455161.1:p.Pro280=
NM_001289155.1:c.845-448C=	NP_001276084.1:n.845-448C=
NM_001289156.1:c.748C=	NP_001276085.1:p.Pro250=
NM_001289157.1:c.715C=	NP_001276086.1:p.Pro239=
NM_002435.2:c.898C=	NP_002426.1:p.Pro300=
XM_011521592.1:c.886C=	XP_011519894.1:p.Pro296=
XM_011521593.1:c.838C=	XP_011519895.1:p.Pro280=
NM_001330372.1:c.838C=	NP_001317301.1:p.Pro280=
XM_017022208.1:c.785-448C=	XP_016877697.1:n.785-448C=
XM_017022209.2:c.695-448C=	XP_016877698.1:n.695-448C=
NM_002435.3:c.898C= MANE Select	NP_002426.1:p.Pro300=
NM_001289155.2:c.845-448C=	NP_001276084.1:n.845-448C=
NM_001289156.2:c.748C=	NP_001276085.1:p.Pro250=
NM_001289157.2:c.715C=	NP_001276086.1:p.Pro239=
NM_001330372.2:c.838C=	NP_001317301.1:p.Pro280=