Canonical Allele Identifier: CA1240217191

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312695C= , CM000664.2:g.27312695C=	GRCh38
NC_000002.11:g.27535562C= , CM000664.1:g.27535562C=	GRCh37
NC_000002.10:g.27389066C=	NCBI36
NG_008075.1:g.14870G=
NG_033055.1:g.569G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.264G= MANE Select	ENSP00000369383.1:p.Lys88=
ENST00000233545.6:c.264G=	ENSP00000233545.2:p.Lys88=
ENST00000357186.10:c.96G=	ENSP00000349713.6:p.Lys32=
ENST00000380044.5:c.264G=	ENSP00000369383.1:p.Lys88=
ENST00000402310.5:c.264G=	ENSP00000383955.1:p.Lys88=
ENST00000402722.5:c.229G=	ENSP00000386000.1:p.Asp77=
ENST00000403262.6:c.264G=	ENSP00000385671.1:p.Lys88=
ENST00000405076.5:c.186+299G=	ENSP00000385175.1:n.186+299G=
ENST00000405983.5:c.309G=	ENSP00000384586.1:p.Lys103=
ENST00000415514.5:c.*65G=	ENSP00000388043.1:n.*65G=
ENST00000426513.6:c.229G=	ENSP00000403824.2:p.Asp77=
ENST00000428910.5:c.186G=	ENSP00000405235.1:p.Lys62=
ENST00000430991.5:c.194G=
ENST00000475085.1:n.292G=
ENST00000616446.1:n.241G=
ENST00000616707.1:n.693G=
ENST00000617583.4:n.290G=
ENST00000621183.4:n.320G=
ENST00000621470.4:n.280G=
ENST00000622003.4:n.437G=
NM_002437.4:c.264G=	NP_002428.1:p.Lys88=
XM_005264326.2:c.264G=	XP_005264383.1:p.Lys88=
XM_005264327.2:c.105G=	XP_005264384.1:p.Lys35=
XM_006712021.2:c.216G=	XP_006712084.1:p.Lys72=
XM_005264326.4:c.264G=	XP_005264383.1:p.Lys88=
XM_006712021.3:c.216G=	XP_006712084.1:p.Lys72=
XM_017004150.1:c.246G=	XP_016859639.1:p.Lys82=
XM_017004151.1:c.216G=	XP_016859640.1:p.Lys72=
XM_017004152.1:c.105G=	XP_016859641.1:p.Lys35=
XM_024452913.1:c.216G=	XP_024308681.1:p.Lys72=
NM_002437.5:c.264G= MANE Select	NP_002428.1:p.Lys88=