Canonical Allele Identifier: CA2658326238

Gene: MPV17

Linked Data

• gnomAD v4: 2-27312388-GGCCCTACCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312391_27312399del , CM000664.2:g.27312391_27312399del	GRCh38
NC_000002.11:g.27535259_27535267del , CM000664.1:g.27535259_27535267del	GRCh37
NC_000002.10:g.27388763_27388771del	NCBI36
NG_008075.1:g.15167_15175del
NG_033055.1:g.866_874del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.375+97_375+105del MANE Select	ENSP00000369383.1:n.375+97_375+105del
ENST00000233545.6:c.375+97_375+105del	ENSP00000233545.2:n.375+97_375+105del
ENST00000357186.10:c.207+97_207+105del	ENSP00000349713.6:n.207+97_207+105del
ENST00000380044.5:c.375+97_375+105del	ENSP00000369383.1:n.375+97_375+105del
ENST00000402310.5:c.375+97_375+105del	ENSP00000383955.1:n.375+97_375+105del
ENST00000402722.5:c.*40+97_*40+105del	ENSP00000386000.1:n.*40+97_*40+105del
ENST00000403262.6:c.375+97_375+105del	ENSP00000385671.1:n.375+97_375+105del
ENST00000405076.5:c.187-151_187-143del	ENSP00000385175.1:n.187-151_187-143del
ENST00000405983.5:c.420+97_420+105del	ENSP00000384586.1:n.420+97_420+105del
ENST00000415514.5:c.*176+97_*176+105del	ENSP00000388043.1:n.*176+97_*176+105del
ENST00000426513.6:c.*40+97_*40+105del	ENSP00000403824.2:n.*40+97_*40+105del
ENST00000428910.5:c.297+97_297+105del	ENSP00000405235.1:n.297+97_297+105del
ENST00000430991.5:c.210-151_210-143del
ENST00000475085.1:n.403+97_403+105del
ENST00000616446.1:n.449_457del
ENST00000616707.1:n.991_999del
ENST00000617583.4:n.498_506del
ENST00000620797.4:n.48+9_48+17del
ENST00000621183.4:n.528_536del
ENST00000621470.4:n.488_496del
ENST00000622003.4:n.645_653del
NM_002437.4:c.375+97_375+105del	NP_002428.1:n.375+97_375+105del
XM_005264326.2:c.375+97_375+105del	XP_005264383.1:n.375+97_375+105del
XM_005264327.2:c.216+97_216+105del	XP_005264384.1:n.216+97_216+105del
XM_006712021.2:c.327+97_327+105del	XP_006712084.1:n.327+97_327+105del
XM_005264326.4:c.375+97_375+105del	XP_005264383.1:n.375+97_375+105del
XM_006712021.3:c.327+97_327+105del	XP_006712084.1:n.327+97_327+105del
XM_017004150.1:c.357+97_357+105del	XP_016859639.1:n.357+97_357+105del
XM_017004151.1:c.327+97_327+105del	XP_016859640.1:n.327+97_327+105del
XM_017004152.1:c.216+97_216+105del	XP_016859641.1:n.216+97_216+105del
XM_024452913.1:c.327+97_327+105del	XP_024308681.1:n.327+97_327+105del
NM_002437.5:c.375+97_375+105del MANE Select	NP_002428.1:n.375+97_375+105del