Canonical Allele Identifier: CA663470628

Gene: MPP7

Linked Data

• dbSNP Id: rs1390299665
• gnomAD v3: 10-28094059-G-GCTAA
• gnomAD v4: 10-28094059-G-GCTAA
• MyVariant Identifiers: chr10:g.28382988_28382989insCTAA (hg19) ; chr10:g.28094059_28094060insCTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28094061_28094064dup , CM000672.2:g.28094061_28094064dup	GRCh38
NC_000010.10:g.28382990_28382993dup , CM000672.1:g.28382990_28382993dup	GRCh37
NC_000010.9:g.28422996_28422999dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683449.1:c.953-4222_953-4219dup MANE Select	ENSP00000507917.1:n.953-4222_953-4219dup
ENST00000337532.9:c.953-4222_953-4219dup	ENSP00000337907.5:n.953-4222_953-4219dup
ENST00000375719.7:c.953-4222_953-4219dup	ENSP00000364871.3:n.953-4222_953-4219dup
ENST00000375732.5:c.953-4222_953-4219dup	ENSP00000364884.1:n.953-4222_953-4219dup
ENST00000441595.2:c.236-4222_236-4219dup	ENSP00000398319.1:n.236-4222_236-4219dup
ENST00000496637.6:c.953-4222_953-4219dup	ENSP00000473899.1:n.953-4222_953-4219dup
NM_173496.3:c.953-4222_953-4219dup	NP_775767.2:n.953-4222_953-4219dup
XM_005252367.2:c.953-4222_953-4219dup	XP_005252424.1:n.953-4222_953-4219dup
XM_005252368.2:c.953-4222_953-4219dup	XP_005252425.1:n.953-4222_953-4219dup
XM_011519337.1:c.953-4222_953-4219dup	XP_011517639.1:n.953-4222_953-4219dup
XM_011519338.1:c.578-4222_578-4219dup	XP_011517640.1:n.578-4222_578-4219dup
XM_011519339.1:c.578-4222_578-4219dup	XP_011517641.1:n.578-4222_578-4219dup
XR_930470.1:n.1248-4222_1248-4219dup
NM_001318170.1:c.953-4222_953-4219dup	NP_001305099.1:n.953-4222_953-4219dup
NM_173496.4:c.953-4222_953-4219dup	NP_775767.2:n.953-4222_953-4219dup
NR_134517.1:n.1290-4222_1290-4219dup
NR_134518.1:n.1171-4222_1171-4219dup
XM_011519337.2:c.953-4222_953-4219dup	XP_011517639.1:n.953-4222_953-4219dup
XM_011519338.2:c.578-4222_578-4219dup	XP_011517640.1:n.578-4222_578-4219dup
XM_017015741.1:c.1196-4222_1196-4219dup	XP_016871230.1:n.1196-4222_1196-4219dup
XM_017015742.1:c.947-4222_947-4219dup	XP_016871231.1:n.947-4222_947-4219dup
NM_001318170.2:c.953-4222_953-4219dup MANE Select	NP_001305099.1:n.953-4222_953-4219dup
NM_173496.5:c.953-4222_953-4219dup	NP_775767.2:n.953-4222_953-4219dup
NR_134517.2:n.1288-4222_1288-4219dup
NR_134518.2:n.1169-4222_1169-4219dup