Canonical Allele Identifier: CA346209118

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535866A>C (hg19) ; chr2:g.27312999A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312999A>C , CM000664.2:g.27312999A>C	GRCh38
NC_000002.11:g.27535866A>C , CM000664.1:g.27535866A>C	GRCh37
NC_000002.10:g.27389370A>C	NCBI36
NG_008075.1:g.14566T>G
NG_033055.1:g.265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.181T>G MANE Select	ENSP00000369383.1:p.Phe61Val
ENST00000233545.6:c.181T>G	ENSP00000233545.2:p.Phe61Val
ENST00000357186.10:c.19-227T>G	ENSP00000349713.6:n.19-227T>G
ENST00000380044.5:c.181T>G	ENSP00000369383.1:p.Phe61Val
ENST00000402310.5:c.181T>G	ENSP00000383955.1:p.Phe61Val
ENST00000402722.5:c.146T>G	ENSP00000386000.1:p.Leu49Arg
ENST00000403262.6:c.181T>G	ENSP00000385671.1:p.Phe61Val
ENST00000405076.5:c.181T>G	ENSP00000385175.1:p.Phe61Val
ENST00000405983.5:c.226T>G	ENSP00000384586.1:p.Phe76Val
ENST00000415514.5:c.228-227T>G	ENSP00000388043.1:n.228-227T>G
ENST00000426513.6:c.146T>G	ENSP00000403824.2:p.Leu49Arg
ENST00000428910.5:c.103T>G	ENSP00000405235.1:p.Phe35Val
ENST00000430991.5:c.111T>G
ENST00000616446.1:n.158T>G
ENST00000616707.1:n.389T>G
ENST00000617583.4:n.207T>G
ENST00000621183.4:n.237T>G
ENST00000621470.4:n.197T>G
ENST00000622003.4:n.354T>G
NM_002437.4:c.181T>G	NP_002428.1:p.Phe61Val
XM_005264326.2:c.181T>G	XP_005264383.1:p.Phe61Val
XM_005264327.2:c.22T>G	XP_005264384.1:p.Phe8Val
XM_006712021.2:c.133T>G	XP_006712084.1:p.Phe45Val
XM_005264326.4:c.181T>G	XP_005264383.1:p.Phe61Val
XM_006712021.3:c.133T>G	XP_006712084.1:p.Phe45Val
XM_017004150.1:c.163T>G	XP_016859639.1:p.Phe55Val
XM_017004151.1:c.133T>G	XP_016859640.1:p.Phe45Val
XM_017004152.1:c.22T>G	XP_016859641.1:p.Phe8Val
XM_024452913.1:c.133T>G	XP_024308681.1:p.Phe45Val
NM_002437.5:c.181T>G MANE Select	NP_002428.1:p.Phe61Val