Canonical Allele Identifier: CA1240215879

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309981C= , CM000664.2:g.27309981C=	GRCh38
NC_000002.11:g.27532849C= , CM000664.1:g.27532849C=	GRCh37
NC_000002.10:g.27386353C=	NCBI36
NG_008075.1:g.17583G=
NG_033055.1:g.3282G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.462G= MANE Select	ENSP00000369383.1:p.Arg154=
ENST00000233545.6:c.462G=	ENSP00000233545.2:p.Arg154=
ENST00000357186.10:c.294G=	ENSP00000349713.6:p.Arg98=
ENST00000380044.5:c.462G=	ENSP00000369383.1:p.Arg154=
ENST00000402310.5:c.409G=	ENSP00000383955.1:p.Val137=
ENST00000402722.5:c.*41G=	ENSP00000386000.1:n.*41G=
ENST00000405076.5:c.273G=	ENSP00000385175.1:p.Arg91=
ENST00000405983.5:c.507G=	ENSP00000384586.1:p.Arg169=
ENST00000415514.5:c.*263G=	ENSP00000388043.1:n.*263G=
ENST00000426513.6:c.*127G=	ENSP00000403824.2:n.*127G=
ENST00000430991.5:c.296G=
ENST00000620797.4:n.135G=
ENST00000621183.4:n.765G=
NM_002437.4:c.462G=	NP_002428.1:p.Arg154=
XM_005264326.2:c.462G=	XP_005264383.1:p.Arg154=
XM_005264327.2:c.303G=	XP_005264384.1:p.Arg101=
XM_006712021.2:c.414G=	XP_006712084.1:p.Arg138=
XM_005264326.4:c.462G=	XP_005264383.1:p.Arg154=
XM_006712021.3:c.414G=	XP_006712084.1:p.Arg138=
XM_017004150.1:c.444G=	XP_016859639.1:p.Arg148=
XM_017004151.1:c.414G=	XP_016859640.1:p.Arg138=
XM_017004152.1:c.303G=	XP_016859641.1:p.Arg101=
XM_024452913.1:c.414G=	XP_024308681.1:p.Arg138=
NM_002437.5:c.462G= MANE Select	NP_002428.1:p.Arg154=