Canonical Allele Identifier: CA1898280627

Gene: MPP7

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28094028C= , CM000672.2:g.28094028C=	GRCh38
NC_000010.10:g.28382957C= , CM000672.1:g.28382957C=	GRCh37
NC_000010.9:g.28422963C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000683449.1:c.953-4187G= MANE Select	ENSP00000507917.1:n.953-4187G=
ENST00000337532.9:c.953-4187G=	ENSP00000337907.5:n.953-4187G=
ENST00000375719.7:c.953-4187G=	ENSP00000364871.3:n.953-4187G=
ENST00000375732.5:c.953-4187G=	ENSP00000364884.1:n.953-4187G=
ENST00000441595.2:c.236-4187G=	ENSP00000398319.1:n.236-4187G=
ENST00000496637.6:c.953-4187G=	ENSP00000473899.1:n.953-4187G=
NM_173496.3:c.953-4187G=	NP_775767.2:n.953-4187G=
XM_005252367.2:c.953-4187G=	XP_005252424.1:n.953-4187G=
XM_005252368.2:c.953-4187G=	XP_005252425.1:n.953-4187G=
XM_011519337.1:c.953-4187G=	XP_011517639.1:n.953-4187G=
XM_011519338.1:c.578-4187G=	XP_011517640.1:n.578-4187G=
XM_011519339.1:c.578-4187G=	XP_011517641.1:n.578-4187G=
XR_930470.1:n.1248-4187G=
NM_001318170.1:c.953-4187G=	NP_001305099.1:n.953-4187G=
NM_173496.4:c.953-4187G=	NP_775767.2:n.953-4187G=
NR_134517.1:n.1290-4187G=
NR_134518.1:n.1171-4187G=
XM_011519337.2:c.953-4187G=	XP_011517639.1:n.953-4187G=
XM_011519338.2:c.578-4187G=	XP_011517640.1:n.578-4187G=
XM_017015741.1:c.1196-4187G=	XP_016871230.1:n.1196-4187G=
XM_017015742.1:c.947-4187G=	XP_016871231.1:n.947-4187G=
NM_001318170.2:c.953-4187G= MANE Select	NP_001305099.1:n.953-4187G=
NM_173496.5:c.953-4187G=	NP_775767.2:n.953-4187G=
NR_134517.2:n.1288-4187G=
NR_134518.2:n.1169-4187G=