Canonical Allele Identifier: CA346209317

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535904C>G (hg19) ; chr2:g.27313037C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313037C>G , CM000664.2:g.27313037C>G	GRCh38
NC_000002.11:g.27535904C>G , CM000664.1:g.27535904C>G	GRCh37
NC_000002.10:g.27389408C>G	NCBI36
NG_008075.1:g.14528G>C
NG_033055.1:g.227G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.143G>C MANE Select	ENSP00000369383.1:p.Arg48Thr
ENST00000233545.6:c.143G>C	ENSP00000233545.2:p.Arg48Thr
ENST00000357186.10:c.19-265G>C	ENSP00000349713.6:n.19-265G>C
ENST00000380044.5:c.143G>C	ENSP00000369383.1:p.Arg48Thr
ENST00000402310.5:c.143G>C	ENSP00000383955.1:p.Arg48Thr
ENST00000402722.5:c.108G>C	ENSP00000386000.1:p.Glu36Asp
ENST00000403262.6:c.143G>C	ENSP00000385671.1:p.Arg48Thr
ENST00000405076.5:c.143G>C	ENSP00000385175.1:p.Arg48Thr
ENST00000405983.5:c.188G>C	ENSP00000384586.1:p.Arg63Thr
ENST00000415514.5:c.228-265G>C	ENSP00000388043.1:n.228-265G>C
ENST00000426513.6:c.108G>C	ENSP00000403824.2:p.Glu36Asp
ENST00000428910.5:c.65G>C	ENSP00000405235.1:p.Arg22Thr
ENST00000430991.5:c.73G>C
ENST00000616446.1:n.120G>C
ENST00000616707.1:n.351G>C
ENST00000617583.4:n.169G>C
ENST00000621183.4:n.199G>C
ENST00000621470.4:n.159G>C
ENST00000622003.4:n.316G>C
NM_002437.4:c.143G>C	NP_002428.1:p.Arg48Thr
XM_005264326.2:c.143G>C	XP_005264383.1:p.Arg48Thr
XM_005264327.2:c.-17G>C	XP_005264384.1:n.-17G>C
XM_006712021.2:c.95G>C	XP_006712084.1:p.Arg32Thr
XM_005264326.4:c.143G>C	XP_005264383.1:p.Arg48Thr
XM_006712021.3:c.95G>C	XP_006712084.1:p.Arg32Thr
XM_017004150.1:c.125G>C	XP_016859639.1:p.Arg42Thr
XM_017004151.1:c.95G>C	XP_016859640.1:p.Arg32Thr
XM_017004152.1:c.-17G>C	XP_016859641.1:n.-17G>C
XM_024452913.1:c.95G>C	XP_024308681.1:p.Arg32Thr
NM_002437.5:c.143G>C MANE Select	NP_002428.1:p.Arg48Thr