Canonical Allele Identifier: CA204551296

Gene: MPP7

Linked Data

• dbSNP Id: rs4317882
• gnomAD v2: 10-28424177-G-A
• gnomAD v3: 10-28135248-G-A
• gnomAD v4: 10-28135248-G-A
• MyVariant Identifiers: chr10:g.28424177G>A (hg19) ; chr10:g.28135248G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.28135248G>A , CM000672.2:g.28135248G>A	GRCh38
NC_000010.10:g.28424177G>A , CM000672.1:g.28424177G>A	GRCh37
NC_000010.9:g.28464183G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000683449.1:c.316-3557C>T MANE Select	ENSP00000507917.1:n.316-3557C>T
ENST00000337532.9:c.316-3557C>T	ENSP00000337907.5:n.316-3557C>T
ENST00000375719.7:c.316-3557C>T	ENSP00000364871.3:n.316-3557C>T
ENST00000375732.5:c.316-3557C>T	ENSP00000364884.1:n.316-3557C>T
ENST00000441595.2:c.157-15041C>T	ENSP00000398319.1:n.157-15041C>T
ENST00000474731.1:n.619-3557C>T
ENST00000481244.5:n.585-3557C>T
ENST00000496637.6:c.316-3557C>T	ENSP00000473899.1:n.316-3557C>T
NM_173496.3:c.316-3557C>T	NP_775767.2:n.316-3557C>T
XM_005252367.2:c.316-3557C>T	XP_005252424.1:n.316-3557C>T
XM_005252368.2:c.316-3557C>T	XP_005252425.1:n.316-3557C>T
XM_005252369.2:c.316-3557C>T	XP_005252426.1:n.316-3557C>T
XM_011519337.1:c.316-3557C>T	XP_011517639.1:n.316-3557C>T
XM_011519338.1:c.-60-3557C>T	XP_011517640.1:n.-60-3557C>T
XM_011519339.1:c.-60-3557C>T	XP_011517641.1:n.-60-3557C>T
XM_011519340.1:c.316-3557C>T	XP_011517642.1:n.316-3557C>T
XM_011519341.1:c.316-3557C>T	XP_011517643.1:n.316-3557C>T
XR_930470.1:n.611-3557C>T
NM_001318170.1:c.316-3557C>T	NP_001305099.1:n.316-3557C>T
NM_173496.4:c.316-3557C>T	NP_775767.2:n.316-3557C>T
NR_134517.1:n.653-3557C>T
NR_134518.1:n.534-3557C>T
XM_005252369.3:c.316-3557C>T	XP_005252426.1:n.316-3557C>T
XM_011519337.2:c.316-3557C>T	XP_011517639.1:n.316-3557C>T
XM_011519338.2:c.-60-3557C>T	XP_011517640.1:n.-60-3557C>T
XM_017015741.1:c.559-3557C>T	XP_016871230.1:n.559-3557C>T
XM_017015742.1:c.310-3557C>T	XP_016871231.1:n.310-3557C>T
XM_017015743.2:c.559-3557C>T	XP_016871232.1:n.559-3557C>T
NM_001318170.2:c.316-3557C>T MANE Select	NP_001305099.1:n.316-3557C>T
NM_173496.5:c.316-3557C>T	NP_775767.2:n.316-3557C>T
NR_134517.2:n.651-3557C>T
NR_134518.2:n.532-3557C>T