Canonical Allele Identifier: CA1240217376

Gene: MPV17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313105G= , CM000664.2:g.27313105G=	GRCh38
NC_000002.11:g.27535972G= , CM000664.1:g.27535972G=	GRCh37
NC_000002.10:g.27389476G=	NCBI36
NG_008075.1:g.14460C=
NG_033055.1:g.159C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.75C= MANE Select	ENSP00000369383.1:p.Ser25=
ENST00000233545.6:c.75C=	ENSP00000233545.2:p.Ser25=
ENST00000357186.10:c.19-333C=	ENSP00000349713.6:n.19-333C=
ENST00000380044.5:c.75C=	ENSP00000369383.1:p.Ser25=
ENST00000402310.5:c.75C=	ENSP00000383955.1:p.Ser25=
ENST00000402722.5:c.71-31C=	ENSP00000386000.1:n.71-31C=
ENST00000403262.6:c.75C=	ENSP00000385671.1:p.Ser25=
ENST00000405076.5:c.75C=	ENSP00000385175.1:p.Ser25=
ENST00000405983.5:c.120C=	ENSP00000384586.1:p.Ser40=
ENST00000415514.5:c.228-333C=	ENSP00000388043.1:n.228-333C=
ENST00000426513.6:c.71-31C=	ENSP00000403824.2:n.71-31C=
ENST00000428910.5:c.-4C=	ENSP00000405235.1:n.-4C=
ENST00000430991.5:c.5C=
ENST00000616446.1:n.52C=
ENST00000616707.1:n.283C=
ENST00000617583.4:n.101C=
ENST00000621183.4:n.131C=
ENST00000621470.4:n.122-31C=
ENST00000622003.4:n.248C=
NM_002437.4:c.75C=	NP_002428.1:p.Ser25=
XM_005264326.2:c.75C=	XP_005264383.1:p.Ser25=
XM_005264327.2:c.-54-31C=	XP_005264384.1:n.-54-31C=
XM_006712021.2:c.27C=	XP_006712084.1:p.Ser9=
XM_005264326.4:c.75C=	XP_005264383.1:p.Ser25=
XM_006712021.3:c.27C=	XP_006712084.1:p.Ser9=
XM_017004150.1:c.57C=	XP_016859639.1:p.Ser19=
XM_017004151.1:c.27C=	XP_016859640.1:p.Ser9=
XM_017004152.1:c.-54-31C=	XP_016859641.1:n.-54-31C=
XM_024452913.1:c.27C=	XP_024308681.1:p.Ser9=
NM_002437.5:c.75C= MANE Select	NP_002428.1:p.Ser25=