Canonical Allele Identifier: CA2187901810

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896222T= , CM000677.2:g.74896222T=	GRCh38
NC_000015.9:g.75188563T= , CM000677.1:g.75188563T=	GRCh37
NC_000015.8:g.72975616T=	NCBI36
NG_008921.1:g.11154T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000352410.9:c.741T= MANE Select	ENSP00000318318.6:p.Gly247=
ENST00000323744.10:c.558T=	ENSP00000318192.6:p.Gly186=
ENST00000352410.8:c.741T=	ENSP00000318318.6:p.Gly247=
ENST00000535694.5:c.591T=	ENSP00000440447.1:p.Gly197=
ENST00000562606.5:c.681T=	ENSP00000457020.1:p.Gly227=
ENST00000562800.5:c.256-1317T=	ENSP00000457619.1:n.256-1317T=
ENST00000563422.5:c.741T=	ENSP00000457885.1:p.Gly247=
ENST00000563786.5:c.681T=	ENSP00000455241.1:p.Gly227=
ENST00000564003.5:c.408T=	ENSP00000454312.1:p.Gly136=
ENST00000566377.5:c.741T=	ENSP00000455405.1:p.Gly247=
ENST00000566556.1:n.789T=
ENST00000567177.1:c.519T=	ENSP00000457013.1:p.Gly173=
ENST00000569931.5:c.681T=	ENSP00000455161.1:p.Gly227=
NM_001289155.1:c.741T=	NP_001276084.1:p.Gly247=
NM_001289156.1:c.591T=	NP_001276085.1:p.Gly197=
NM_001289157.1:c.558T=	NP_001276086.1:p.Gly186=
NM_002435.2:c.741T=	NP_002426.1:p.Gly247=
XM_011521592.1:c.729T=	XP_011519894.1:p.Gly243=
XM_011521593.1:c.681T=	XP_011519895.1:p.Gly227=
NM_001330372.1:c.681T=	NP_001317301.1:p.Gly227=
XM_017022208.1:c.681T=	XP_016877697.1:p.Gly227=
XM_017022209.2:c.591T=	XP_016877698.1:p.Gly197=
NM_002435.3:c.741T= MANE Select	NP_002426.1:p.Gly247=
NM_001289155.2:c.741T=	NP_001276084.1:p.Gly247=
NM_001289156.2:c.591T=	NP_001276085.1:p.Gly197=
NM_001289157.2:c.558T=	NP_001276086.1:p.Gly186=
NM_001330372.2:c.681T=	NP_001317301.1:p.Gly227=