Canonical Allele Identifier: CA1240217031

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312394A= , CM000664.2:g.27312394A=	GRCh38
NC_000002.11:g.27535262A= , CM000664.1:g.27535262A=	GRCh37
NC_000002.10:g.27388766A=	NCBI36
NG_008075.1:g.15170T=
NG_033055.1:g.869T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.375+100T= MANE Select	ENSP00000369383.1:n.375+100T=
ENST00000233545.6:c.375+100T=	ENSP00000233545.2:n.375+100T=
ENST00000357186.10:c.207+100T=	ENSP00000349713.6:n.207+100T=
ENST00000380044.5:c.375+100T=	ENSP00000369383.1:n.375+100T=
ENST00000402310.5:c.375+100T=	ENSP00000383955.1:n.375+100T=
ENST00000402722.5:c.*40+100T=	ENSP00000386000.1:n.*40+100T=
ENST00000403262.6:c.375+100T=	ENSP00000385671.1:n.375+100T=
ENST00000405076.5:c.187-148T=	ENSP00000385175.1:n.187-148T=
ENST00000405983.5:c.420+100T=	ENSP00000384586.1:n.420+100T=
ENST00000415514.5:c.*176+100T=	ENSP00000388043.1:n.*176+100T=
ENST00000426513.6:c.*40+100T=	ENSP00000403824.2:n.*40+100T=
ENST00000428910.5:c.297+100T=	ENSP00000405235.1:n.297+100T=
ENST00000430991.5:c.210-148T=
ENST00000475085.1:n.403+100T=
ENST00000616446.1:n.452T=
ENST00000616707.1:n.994T=
ENST00000617583.4:n.501T=
ENST00000620797.4:n.48+12T=
ENST00000621183.4:n.531T=
ENST00000621470.4:n.491T=
ENST00000622003.4:n.648T=
NM_002437.4:c.375+100T=	NP_002428.1:n.375+100T=
XM_005264326.2:c.375+100T=	XP_005264383.1:n.375+100T=
XM_005264327.2:c.216+100T=	XP_005264384.1:n.216+100T=
XM_006712021.2:c.327+100T=	XP_006712084.1:n.327+100T=
XM_005264326.4:c.375+100T=	XP_005264383.1:n.375+100T=
XM_006712021.3:c.327+100T=	XP_006712084.1:n.327+100T=
XM_017004150.1:c.357+100T=	XP_016859639.1:n.357+100T=
XM_017004151.1:c.327+100T=	XP_016859640.1:n.327+100T=
XM_017004152.1:c.216+100T=	XP_016859641.1:n.216+100T=
XM_024452913.1:c.327+100T=	XP_024308681.1:n.327+100T=
NM_002437.5:c.375+100T= MANE Select	NP_002428.1:n.375+100T=