Canonical Allele Identifier: CA1240217193

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312697T= , CM000664.2:g.27312697T=	GRCh38
NC_000002.11:g.27535564T= , CM000664.1:g.27535564T=	GRCh37
NC_000002.10:g.27389068T=	NCBI36
NG_008075.1:g.14868A=
NG_033055.1:g.567A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.262A= MANE Select	ENSP00000369383.1:p.Lys88=
ENST00000233545.6:c.262A=	ENSP00000233545.2:p.Lys88=
ENST00000357186.10:c.94A=	ENSP00000349713.6:p.Lys32=
ENST00000380044.5:c.262A=	ENSP00000369383.1:p.Lys88=
ENST00000402310.5:c.262A=	ENSP00000383955.1:p.Lys88=
ENST00000402722.5:c.227A=	ENSP00000386000.1:p.Glu76=
ENST00000403262.6:c.262A=	ENSP00000385671.1:p.Lys88=
ENST00000405076.5:c.186+297A=	ENSP00000385175.1:n.186+297A=
ENST00000405983.5:c.307A=	ENSP00000384586.1:p.Lys103=
ENST00000415514.5:c.*63A=	ENSP00000388043.1:n.*63A=
ENST00000426513.6:c.227A=	ENSP00000403824.2:p.Glu76=
ENST00000428910.5:c.184A=	ENSP00000405235.1:p.Lys62=
ENST00000430991.5:c.192A=
ENST00000475085.1:n.290A=
ENST00000616446.1:n.239A=
ENST00000616707.1:n.691A=
ENST00000617583.4:n.288A=
ENST00000621183.4:n.318A=
ENST00000621470.4:n.278A=
ENST00000622003.4:n.435A=
NM_002437.4:c.262A=	NP_002428.1:p.Lys88=
XM_005264326.2:c.262A=	XP_005264383.1:p.Lys88=
XM_005264327.2:c.103A=	XP_005264384.1:p.Lys35=
XM_006712021.2:c.214A=	XP_006712084.1:p.Lys72=
XM_005264326.4:c.262A=	XP_005264383.1:p.Lys88=
XM_006712021.3:c.214A=	XP_006712084.1:p.Lys72=
XM_017004150.1:c.244A=	XP_016859639.1:p.Lys82=
XM_017004151.1:c.214A=	XP_016859640.1:p.Lys72=
XM_017004152.1:c.103A=	XP_016859641.1:p.Lys35=
XM_024452913.1:c.214A=	XP_024308681.1:p.Lys72=
NM_002437.5:c.262A= MANE Select	NP_002428.1:p.Lys88=