Canonical Allele Identifier: CA346209153

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535872A>G (hg19) ; chr2:g.27313005A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313005A>G , CM000664.2:g.27313005A>G	GRCh38
NC_000002.11:g.27535872A>G , CM000664.1:g.27535872A>G	GRCh37
NC_000002.10:g.27389376A>G	NCBI36
NG_008075.1:g.14560T>C
NG_033055.1:g.259T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.175T>C MANE Select	ENSP00000369383.1:p.Cys59Arg
ENST00000233545.6:c.175T>C	ENSP00000233545.2:p.Cys59Arg
ENST00000357186.10:c.19-233T>C	ENSP00000349713.6:n.19-233T>C
ENST00000380044.5:c.175T>C	ENSP00000369383.1:p.Cys59Arg
ENST00000402310.5:c.175T>C	ENSP00000383955.1:p.Cys59Arg
ENST00000402722.5:c.140T>C	ENSP00000386000.1:p.Leu47Pro
ENST00000403262.6:c.175T>C	ENSP00000385671.1:p.Cys59Arg
ENST00000405076.5:c.175T>C	ENSP00000385175.1:p.Cys59Arg
ENST00000405983.5:c.220T>C	ENSP00000384586.1:p.Cys74Arg
ENST00000415514.5:c.228-233T>C	ENSP00000388043.1:n.228-233T>C
ENST00000426513.6:c.140T>C	ENSP00000403824.2:p.Leu47Pro
ENST00000428910.5:c.97T>C	ENSP00000405235.1:p.Cys33Arg
ENST00000430991.5:c.105T>C
ENST00000616446.1:n.152T>C
ENST00000616707.1:n.383T>C
ENST00000617583.4:n.201T>C
ENST00000621183.4:n.231T>C
ENST00000621470.4:n.191T>C
ENST00000622003.4:n.348T>C
NM_002437.4:c.175T>C	NP_002428.1:p.Cys59Arg
XM_005264326.2:c.175T>C	XP_005264383.1:p.Cys59Arg
XM_005264327.2:c.16T>C	XP_005264384.1:p.Cys6Arg
XM_006712021.2:c.127T>C	XP_006712084.1:p.Cys43Arg
XM_005264326.4:c.175T>C	XP_005264383.1:p.Cys59Arg
XM_006712021.3:c.127T>C	XP_006712084.1:p.Cys43Arg
XM_017004150.1:c.157T>C	XP_016859639.1:p.Cys53Arg
XM_017004151.1:c.127T>C	XP_016859640.1:p.Cys43Arg
XM_017004152.1:c.16T>C	XP_016859641.1:p.Cys6Arg
XM_024452913.1:c.127T>C	XP_024308681.1:p.Cys43Arg
NM_002437.5:c.175T>C MANE Select	NP_002428.1:p.Cys59Arg