Canonical Allele Identifier: CA346208571

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535569A>C (hg19) ; chr2:g.27312702A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312702A>C , CM000664.2:g.27312702A>C	GRCh38
NC_000002.11:g.27535569A>C , CM000664.1:g.27535569A>C	GRCh37
NC_000002.10:g.27389073A>C	NCBI36
NG_008075.1:g.14863T>G
NG_033055.1:g.562T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.257T>G MANE Select	ENSP00000369383.1:p.Leu86Arg
ENST00000233545.6:c.257T>G	ENSP00000233545.2:p.Leu86Arg
ENST00000357186.10:c.89T>G	ENSP00000349713.6:p.Leu30Arg
ENST00000380044.5:c.257T>G	ENSP00000369383.1:p.Leu86Arg
ENST00000402310.5:c.257T>G	ENSP00000383955.1:p.Leu86Arg
ENST00000402722.5:c.222T>G	ENSP00000386000.1:p.Thr74=
ENST00000403262.6:c.257T>G	ENSP00000385671.1:p.Leu86Arg
ENST00000405076.5:c.186+292T>G	ENSP00000385175.1:n.186+292T>G
ENST00000405983.5:c.302T>G	ENSP00000384586.1:p.Leu101Arg
ENST00000415514.5:c.*58T>G	ENSP00000388043.1:n.*58T>G
ENST00000426513.6:c.222T>G	ENSP00000403824.2:p.Thr74=
ENST00000428910.5:c.179T>G	ENSP00000405235.1:p.Leu60Arg
ENST00000430991.5:c.187T>G
ENST00000475085.1:n.285T>G
ENST00000616446.1:n.234T>G
ENST00000616707.1:n.686T>G
ENST00000617583.4:n.283T>G
ENST00000621183.4:n.313T>G
ENST00000621470.4:n.273T>G
ENST00000622003.4:n.430T>G
NM_002437.4:c.257T>G	NP_002428.1:p.Leu86Arg
XM_005264326.2:c.257T>G	XP_005264383.1:p.Leu86Arg
XM_005264327.2:c.98T>G	XP_005264384.1:p.Leu33Arg
XM_006712021.2:c.209T>G	XP_006712084.1:p.Leu70Arg
XM_005264326.4:c.257T>G	XP_005264383.1:p.Leu86Arg
XM_006712021.3:c.209T>G	XP_006712084.1:p.Leu70Arg
XM_017004150.1:c.239T>G	XP_016859639.1:p.Leu80Arg
XM_017004151.1:c.209T>G	XP_016859640.1:p.Leu70Arg
XM_017004152.1:c.98T>G	XP_016859641.1:p.Leu33Arg
XM_024452913.1:c.209T>G	XP_024308681.1:p.Leu70Arg
NM_002437.5:c.257T>G MANE Select	NP_002428.1:p.Leu86Arg