Canonical Allele Identifier: CA346208521

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535560A>C (hg19) ; chr2:g.27312693A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312693A>C , CM000664.2:g.27312693A>C	GRCh38
NC_000002.11:g.27535560A>C , CM000664.1:g.27535560A>C	GRCh37
NC_000002.10:g.27389064A>C	NCBI36
NG_008075.1:g.14872T>G
NG_033055.1:g.571T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.266T>G MANE Select	ENSP00000369383.1:p.Met89Arg
ENST00000233545.6:c.266T>G	ENSP00000233545.2:p.Met89Arg
ENST00000357186.10:c.98T>G	ENSP00000349713.6:p.Met33Arg
ENST00000380044.5:c.266T>G	ENSP00000369383.1:p.Met89Arg
ENST00000402310.5:c.266T>G	ENSP00000383955.1:p.Met89Arg
ENST00000402722.5:c.231T>G	ENSP00000386000.1:p.Asp77Glu
ENST00000403262.6:c.266T>G	ENSP00000385671.1:p.Met89Arg
ENST00000405076.5:c.186+301T>G	ENSP00000385175.1:n.186+301T>G
ENST00000405983.5:c.311T>G	ENSP00000384586.1:p.Met104Arg
ENST00000415514.5:c.*67T>G	ENSP00000388043.1:n.*67T>G
ENST00000426513.6:c.231T>G	ENSP00000403824.2:p.Asp77Glu
ENST00000428910.5:c.188T>G	ENSP00000405235.1:p.Met63Arg
ENST00000430991.5:c.196T>G
ENST00000475085.1:n.294T>G
ENST00000616446.1:n.243T>G
ENST00000616707.1:n.695T>G
ENST00000617583.4:n.292T>G
ENST00000621183.4:n.322T>G
ENST00000621470.4:n.282T>G
ENST00000622003.4:n.439T>G
NM_002437.4:c.266T>G	NP_002428.1:p.Met89Arg
XM_005264326.2:c.266T>G	XP_005264383.1:p.Met89Arg
XM_005264327.2:c.107T>G	XP_005264384.1:p.Met36Arg
XM_006712021.2:c.218T>G	XP_006712084.1:p.Met73Arg
XM_005264326.4:c.266T>G	XP_005264383.1:p.Met89Arg
XM_006712021.3:c.218T>G	XP_006712084.1:p.Met73Arg
XM_017004150.1:c.248T>G	XP_016859639.1:p.Met83Arg
XM_017004151.1:c.218T>G	XP_016859640.1:p.Met73Arg
XM_017004152.1:c.107T>G	XP_016859641.1:p.Met36Arg
XM_024452913.1:c.218T>G	XP_024308681.1:p.Met73Arg
NM_002437.5:c.266T>G MANE Select	NP_002428.1:p.Met89Arg