Canonical Allele Identifier: CA346209311

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535903T>C (hg19) ; chr2:g.27313036T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313036T>C , CM000664.2:g.27313036T>C	GRCh38
NC_000002.11:g.27535903T>C , CM000664.1:g.27535903T>C	GRCh37
NC_000002.10:g.27389407T>C	NCBI36
NG_008075.1:g.14529A>G
NG_033055.1:g.228A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.144A>G MANE Select	ENSP00000369383.1:p.Arg48=
ENST00000233545.6:c.144A>G	ENSP00000233545.2:p.Arg48=
ENST00000357186.10:c.19-264A>G	ENSP00000349713.6:n.19-264A>G
ENST00000380044.5:c.144A>G	ENSP00000369383.1:p.Arg48=
ENST00000402310.5:c.144A>G	ENSP00000383955.1:p.Arg48=
ENST00000402722.5:c.109A>G	ENSP00000386000.1:p.Arg37Gly
ENST00000403262.6:c.144A>G	ENSP00000385671.1:p.Arg48=
ENST00000405076.5:c.144A>G	ENSP00000385175.1:p.Arg48=
ENST00000405983.5:c.189A>G	ENSP00000384586.1:p.Arg63=
ENST00000415514.5:c.228-264A>G	ENSP00000388043.1:n.228-264A>G
ENST00000426513.6:c.109A>G	ENSP00000403824.2:p.Arg37Gly
ENST00000428910.5:c.66A>G	ENSP00000405235.1:p.Arg22=
ENST00000430991.5:c.74A>G
ENST00000616446.1:n.121A>G
ENST00000616707.1:n.352A>G
ENST00000617583.4:n.170A>G
ENST00000621183.4:n.200A>G
ENST00000621470.4:n.160A>G
ENST00000622003.4:n.317A>G
NM_002437.4:c.144A>G	NP_002428.1:p.Arg48=
XM_005264326.2:c.144A>G	XP_005264383.1:p.Arg48=
XM_005264327.2:c.-16A>G	XP_005264384.1:n.-16A>G
XM_006712021.2:c.96A>G	XP_006712084.1:p.Arg32=
XM_005264326.4:c.144A>G	XP_005264383.1:p.Arg48=
XM_006712021.3:c.96A>G	XP_006712084.1:p.Arg32=
XM_017004150.1:c.126A>G	XP_016859639.1:p.Arg42=
XM_017004151.1:c.96A>G	XP_016859640.1:p.Arg32=
XM_017004152.1:c.-16A>G	XP_016859641.1:n.-16A>G
XM_024452913.1:c.96A>G	XP_024308681.1:p.Arg32=
NM_002437.5:c.144A>G MANE Select	NP_002428.1:p.Arg48=