Canonical Allele Identifier: CA1240217149

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312630C= , CM000664.2:g.27312630C=	GRCh38
NC_000002.11:g.27535497C= , CM000664.1:g.27535497C=	GRCh37
NC_000002.10:g.27389001C=	NCBI36
NG_008075.1:g.14935G=
NG_033055.1:g.634G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.280-41G= MANE Select	ENSP00000369383.1:n.280-41G=
ENST00000233545.6:c.280-41G=	ENSP00000233545.2:n.280-41G=
ENST00000357186.10:c.112-41G=	ENSP00000349713.6:n.112-41G=
ENST00000380044.5:c.280-41G=	ENSP00000369383.1:n.280-41G=
ENST00000402310.5:c.280-41G=	ENSP00000383955.1:n.280-41G=
ENST00000402722.5:c.245-41G=	ENSP00000386000.1:n.245-41G=
ENST00000403262.6:c.280-41G=	ENSP00000385671.1:n.280-41G=
ENST00000405076.5:c.186+364G=	ENSP00000385175.1:n.186+364G=
ENST00000405983.5:c.325-41G=	ENSP00000384586.1:n.325-41G=
ENST00000415514.5:c.*81-41G=	ENSP00000388043.1:n.*81-41G=
ENST00000426513.6:c.245-41G=	ENSP00000403824.2:n.245-41G=
ENST00000428910.5:c.202-41G=	ENSP00000405235.1:n.202-41G=
ENST00000430991.5:c.209+50G=
ENST00000475085.1:n.308-41G=
ENST00000616446.1:n.257-41G=
ENST00000616707.1:n.758G=
ENST00000617583.4:n.306-41G=
ENST00000621183.4:n.336-41G=
ENST00000621470.4:n.296-41G=
ENST00000622003.4:n.453-41G=
NM_002437.4:c.280-41G=	NP_002428.1:n.280-41G=
XM_005264326.2:c.280-41G=	XP_005264383.1:n.280-41G=
XM_005264327.2:c.121-41G=	XP_005264384.1:n.121-41G=
XM_006712021.2:c.232-41G=	XP_006712084.1:n.232-41G=
XM_005264326.4:c.280-41G=	XP_005264383.1:n.280-41G=
XM_006712021.3:c.232-41G=	XP_006712084.1:n.232-41G=
XM_017004150.1:c.262-41G=	XP_016859639.1:n.262-41G=
XM_017004151.1:c.232-41G=	XP_016859640.1:n.232-41G=
XM_017004152.1:c.121-41G=	XP_016859641.1:n.121-41G=
XM_024452913.1:c.232-41G=	XP_024308681.1:n.232-41G=
NM_002437.5:c.280-41G= MANE Select	NP_002428.1:n.280-41G=