Canonical Allele Identifier: CA1240217355

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313054A= , CM000664.2:g.27313054A=	GRCh38
NC_000002.11:g.27535921A= , CM000664.1:g.27535921A=	GRCh37
NC_000002.10:g.27389425A=	NCBI36
NG_008075.1:g.14511T=
NG_033055.1:g.210T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.126T= MANE Select	ENSP00000369383.1:p.Gly42=
ENST00000233545.6:c.126T=	ENSP00000233545.2:p.Gly42=
ENST00000357186.10:c.19-282T=	ENSP00000349713.6:n.19-282T=
ENST00000380044.5:c.126T=	ENSP00000369383.1:p.Gly42=
ENST00000402310.5:c.126T=	ENSP00000383955.1:p.Gly42=
ENST00000402722.5:c.91T=	ENSP00000386000.1:p.Ser31=
ENST00000403262.6:c.126T=	ENSP00000385671.1:p.Gly42=
ENST00000405076.5:c.126T=	ENSP00000385175.1:p.Gly42=
ENST00000405983.5:c.171T=	ENSP00000384586.1:p.Gly57=
ENST00000415514.5:c.228-282T=	ENSP00000388043.1:n.228-282T=
ENST00000426513.6:c.91T=	ENSP00000403824.2:p.Ser31=
ENST00000428910.5:c.48T=	ENSP00000405235.1:p.Gly16=
ENST00000430991.5:c.56T=
ENST00000616446.1:n.103T=
ENST00000616707.1:n.334T=
ENST00000617583.4:n.152T=
ENST00000621183.4:n.182T=
ENST00000621470.4:n.142T=
ENST00000622003.4:n.299T=
NM_002437.4:c.126T=	NP_002428.1:p.Gly42=
XM_005264326.2:c.126T=	XP_005264383.1:p.Gly42=
XM_005264327.2:c.-34T=	XP_005264384.1:n.-34T=
XM_006712021.2:c.78T=	XP_006712084.1:p.Gly26=
XM_005264326.4:c.126T=	XP_005264383.1:p.Gly42=
XM_006712021.3:c.78T=	XP_006712084.1:p.Gly26=
XM_017004150.1:c.108T=	XP_016859639.1:p.Gly36=
XM_017004151.1:c.78T=	XP_016859640.1:p.Gly26=
XM_017004152.1:c.-34T=	XP_016859641.1:n.-34T=
XM_024452913.1:c.78T=	XP_024308681.1:p.Gly26=
NM_002437.5:c.126T= MANE Select	NP_002428.1:p.Gly42=