Canonical Allele Identifier: CA1240216767

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27311853G= , CM000664.2:g.27311853G=	GRCh38
NC_000002.11:g.27534721G= , CM000664.1:g.27534721G=	GRCh37
NC_000002.10:g.27388225G=	NCBI36
NG_008075.1:g.15711C=
NG_033055.1:g.1410C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.461+46C= MANE Select	ENSP00000369383.1:n.461+46C=
ENST00000233545.6:c.461+46C=	ENSP00000233545.2:n.461+46C=
ENST00000357186.10:c.293+46C=	ENSP00000349713.6:n.293+46C=
ENST00000380044.5:c.461+46C=	ENSP00000369383.1:n.461+46C=
ENST00000402310.5:c.408+361C=	ENSP00000383955.1:n.408+361C=
ENST00000402722.5:c.*40+641C=	ENSP00000386000.1:n.*40+641C=
ENST00000403262.6:c.461+46C=	ENSP00000385671.1:n.461+46C=
ENST00000405076.5:c.272+46C=	ENSP00000385175.1:n.272+46C=
ENST00000405983.5:c.506+46C=	ENSP00000384586.1:n.506+46C=
ENST00000415514.5:c.*262+46C=	ENSP00000388043.1:n.*262+46C=
ENST00000426513.6:c.*126+46C=	ENSP00000403824.2:n.*126+46C=
ENST00000430991.5:c.295+46C=
ENST00000616707.1:n.1535C=
ENST00000620797.4:n.134+46C=
ENST00000621183.4:n.764+46C=
NM_002437.4:c.461+46C=	NP_002428.1:n.461+46C=
XM_005264326.2:c.461+46C=	XP_005264383.1:n.461+46C=
XM_005264327.2:c.302+46C=	XP_005264384.1:n.302+46C=
XM_006712021.2:c.413+46C=	XP_006712084.1:n.413+46C=
XM_005264326.4:c.461+46C=	XP_005264383.1:n.461+46C=
XM_006712021.3:c.413+46C=	XP_006712084.1:n.413+46C=
XM_017004150.1:c.443+46C=	XP_016859639.1:n.443+46C=
XM_017004151.1:c.413+46C=	XP_016859640.1:n.413+46C=
XM_017004152.1:c.302+46C=	XP_016859641.1:n.302+46C=
XM_024452913.1:c.413+46C=	XP_024308681.1:n.413+46C=
NM_002437.5:c.461+46C= MANE Select	NP_002428.1:n.461+46C=