Canonical Allele Identifier: CA2187901736

Gene: MPI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74896165C= , CM000677.2:g.74896165C=	GRCh38
NC_000015.9:g.75188506C= , CM000677.1:g.75188506C=	GRCh37
NC_000015.8:g.72975559C=	NCBI36
NG_008921.1:g.11097C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352410.9:c.684C= MANE Select	ENSP00000318318.6:p.Asn228=
ENST00000323744.10:c.501C=	ENSP00000318192.6:p.Asn167=
ENST00000352410.8:c.684C=	ENSP00000318318.6:p.Asn228=
ENST00000535694.5:c.534C=	ENSP00000440447.1:p.Asn178=
ENST00000561470.5:c.*580C=	ENSP00000454267.1:n.*580C=
ENST00000562606.5:c.624C=	ENSP00000457020.1:p.Asn208=
ENST00000562800.5:c.256-1374C=	ENSP00000457619.1:n.256-1374C=
ENST00000563422.5:c.684C=	ENSP00000457885.1:p.Asn228=
ENST00000563786.5:c.624C=	ENSP00000455241.1:p.Asn208=
ENST00000564003.5:c.351C=	ENSP00000454312.1:p.Asn117=
ENST00000566377.5:c.684C=	ENSP00000455405.1:p.Asn228=
ENST00000566556.1:n.732C=
ENST00000567177.1:c.462C=	ENSP00000457013.1:p.Asn154=
ENST00000569931.5:c.624C=	ENSP00000455161.1:p.Asn208=
NM_001289155.1:c.684C=	NP_001276084.1:p.Asn228=
NM_001289156.1:c.534C=	NP_001276085.1:p.Asn178=
NM_001289157.1:c.501C=	NP_001276086.1:p.Asn167=
NM_002435.2:c.684C=	NP_002426.1:p.Asn228=
XM_011521592.1:c.672C=	XP_011519894.1:p.Asn224=
XM_011521593.1:c.624C=	XP_011519895.1:p.Asn208=
NM_001330372.1:c.624C=	NP_001317301.1:p.Asn208=
XM_017022208.1:c.624C=	XP_016877697.1:p.Asn208=
XM_017022209.2:c.534C=	XP_016877698.1:p.Asn178=
NM_002435.3:c.684C= MANE Select	NP_002426.1:p.Asn228=
NM_001289155.2:c.684C=	NP_001276084.1:p.Asn228=
NM_001289156.2:c.534C=	NP_001276085.1:p.Asn178=
NM_001289157.2:c.501C=	NP_001276086.1:p.Asn167=
NM_001330372.2:c.624C=	NP_001317301.1:p.Asn208=