Canonical Allele Identifier: CA346209387

Gene: MPV17

Linked Data

• COSMIC: COSM5676841 ; COSM5676842
• MyVariant Identifiers: chr2:g.27535916T>C (hg19) ; chr2:g.27313049T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313049T>C , CM000664.2:g.27313049T>C	GRCh38
NC_000002.11:g.27535916T>C , CM000664.1:g.27535916T>C	GRCh37
NC_000002.10:g.27389420T>C	NCBI36
NG_008075.1:g.14516A>G
NG_033055.1:g.215A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.131A>G MANE Select	ENSP00000369383.1:p.Gln44Arg
ENST00000233545.6:c.131A>G	ENSP00000233545.2:p.Gln44Arg
ENST00000357186.10:c.19-277A>G	ENSP00000349713.6:n.19-277A>G
ENST00000380044.5:c.131A>G	ENSP00000369383.1:p.Gln44Arg
ENST00000402310.5:c.131A>G	ENSP00000383955.1:p.Gln44Arg
ENST00000402722.5:c.96A>G	ENSP00000386000.1:p.Ala32=
ENST00000403262.6:c.131A>G	ENSP00000385671.1:p.Gln44Arg
ENST00000405076.5:c.131A>G	ENSP00000385175.1:p.Gln44Arg
ENST00000405983.5:c.176A>G	ENSP00000384586.1:p.Gln59Arg
ENST00000415514.5:c.228-277A>G	ENSP00000388043.1:n.228-277A>G
ENST00000426513.6:c.96A>G	ENSP00000403824.2:p.Ala32=
ENST00000428910.5:c.53A>G	ENSP00000405235.1:p.Gln18Arg
ENST00000430991.5:c.61A>G
ENST00000616446.1:n.108A>G
ENST00000616707.1:n.339A>G
ENST00000617583.4:n.157A>G
ENST00000621183.4:n.187A>G
ENST00000621470.4:n.147A>G
ENST00000622003.4:n.304A>G
NM_002437.4:c.131A>G	NP_002428.1:p.Gln44Arg
XM_005264326.2:c.131A>G	XP_005264383.1:p.Gln44Arg
XM_005264327.2:c.-29A>G	XP_005264384.1:n.-29A>G
XM_006712021.2:c.83A>G	XP_006712084.1:p.Gln28Arg
XM_005264326.4:c.131A>G	XP_005264383.1:p.Gln44Arg
XM_006712021.3:c.83A>G	XP_006712084.1:p.Gln28Arg
XM_017004150.1:c.113A>G	XP_016859639.1:p.Gln38Arg
XM_017004151.1:c.83A>G	XP_016859640.1:p.Gln28Arg
XM_017004152.1:c.-29A>G	XP_016859641.1:n.-29A>G
XM_024452913.1:c.83A>G	XP_024308681.1:p.Gln28Arg
NM_002437.5:c.131A>G MANE Select	NP_002428.1:p.Gln44Arg