Canonical Allele Identifier: CA1240217095

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312495C= , CM000664.2:g.27312495C=	GRCh38
NC_000002.11:g.27535362C= , CM000664.1:g.27535362C=	GRCh37
NC_000002.10:g.27388866C=	NCBI36
NG_008075.1:g.15070G=
NG_033055.1:g.769G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.374G= MANE Select	ENSP00000369383.1:p.Arg125=
ENST00000233545.6:c.374G=	ENSP00000233545.2:p.Arg125=
ENST00000357186.10:c.206G=	ENSP00000349713.6:p.Arg69=
ENST00000380044.5:c.374G=	ENSP00000369383.1:p.Arg125=
ENST00000402310.5:c.374G=	ENSP00000383955.1:p.Arg125=
ENST00000402722.5:c.*39G=	ENSP00000386000.1:n.*39G=
ENST00000403262.6:c.374G=	ENSP00000385671.1:p.Arg125=
ENST00000405076.5:c.187-249G=	ENSP00000385175.1:n.187-249G=
ENST00000405983.5:c.419G=	ENSP00000384586.1:p.Arg140=
ENST00000415514.5:c.*175G=	ENSP00000388043.1:n.*175G=
ENST00000426513.6:c.*39G=	ENSP00000403824.2:n.*39G=
ENST00000428910.5:c.296G=	ENSP00000405235.1:p.Arg99=
ENST00000430991.5:c.209+185G=
ENST00000475085.1:n.402G=
ENST00000616446.1:n.351G=
ENST00000616707.1:n.893G=
ENST00000617583.4:n.400G=
ENST00000621183.4:n.430G=
ENST00000621470.4:n.390G=
ENST00000622003.4:n.547G=
NM_002437.4:c.374G=	NP_002428.1:p.Arg125=
XM_005264326.2:c.374G=	XP_005264383.1:p.Arg125=
XM_005264327.2:c.215G=	XP_005264384.1:p.Arg72=
XM_006712021.2:c.326G=	XP_006712084.1:p.Arg109=
XM_005264326.4:c.374G=	XP_005264383.1:p.Arg125=
XM_006712021.3:c.326G=	XP_006712084.1:p.Arg109=
XM_017004150.1:c.356G=	XP_016859639.1:p.Arg119=
XM_017004151.1:c.326G=	XP_016859640.1:p.Arg109=
XM_017004152.1:c.215G=	XP_016859641.1:p.Arg72=
XM_024452913.1:c.326G=	XP_024308681.1:p.Arg109=
NM_002437.5:c.374G= MANE Select	NP_002428.1:p.Arg125=