Canonical Allele Identifier: CA346209501

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535961A>C (hg19) ; chr2:g.27313094A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313094A>C , CM000664.2:g.27313094A>C	GRCh38
NC_000002.11:g.27535961A>C , CM000664.1:g.27535961A>C	GRCh37
NC_000002.10:g.27389465A>C	NCBI36
NG_008075.1:g.14471T>G
NG_033055.1:g.170T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.86T>G MANE Select	ENSP00000369383.1:p.Leu29Arg
ENST00000233545.6:c.86T>G	ENSP00000233545.2:p.Leu29Arg
ENST00000357186.10:c.19-322T>G	ENSP00000349713.6:n.19-322T>G
ENST00000380044.5:c.86T>G	ENSP00000369383.1:p.Leu29Arg
ENST00000402310.5:c.86T>G	ENSP00000383955.1:p.Leu29Arg
ENST00000402722.5:c.71-20T>G	ENSP00000386000.1:n.71-20T>G
ENST00000403262.6:c.86T>G	ENSP00000385671.1:p.Leu29Arg
ENST00000405076.5:c.86T>G	ENSP00000385175.1:p.Leu29Arg
ENST00000405983.5:c.131T>G	ENSP00000384586.1:p.Leu44Arg
ENST00000415514.5:c.228-322T>G	ENSP00000388043.1:n.228-322T>G
ENST00000426513.6:c.71-20T>G	ENSP00000403824.2:n.71-20T>G
ENST00000428910.5:c.8T>G	ENSP00000405235.1:p.Leu3Arg
ENST00000430991.5:c.16T>G
ENST00000616446.1:n.63T>G
ENST00000616707.1:n.294T>G
ENST00000617583.4:n.112T>G
ENST00000621183.4:n.142T>G
ENST00000621470.4:n.122-20T>G
ENST00000622003.4:n.259T>G
NM_002437.4:c.86T>G	NP_002428.1:p.Leu29Arg
XM_005264326.2:c.86T>G	XP_005264383.1:p.Leu29Arg
XM_005264327.2:c.-54-20T>G	XP_005264384.1:n.-54-20T>G
XM_006712021.2:c.38T>G	XP_006712084.1:p.Leu13Arg
XM_005264326.4:c.86T>G	XP_005264383.1:p.Leu29Arg
XM_006712021.3:c.38T>G	XP_006712084.1:p.Leu13Arg
XM_017004150.1:c.68T>G	XP_016859639.1:p.Leu23Arg
XM_017004151.1:c.38T>G	XP_016859640.1:p.Leu13Arg
XM_017004152.1:c.-54-20T>G	XP_016859641.1:n.-54-20T>G
XM_024452913.1:c.38T>G	XP_024308681.1:p.Leu13Arg
NM_002437.5:c.86T>G MANE Select	NP_002428.1:p.Leu29Arg