Canonical Allele Identifier: CA346209350

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535910T>C (hg19) ; chr2:g.27313043T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313043T>C , CM000664.2:g.27313043T>C	GRCh38
NC_000002.11:g.27535910T>C , CM000664.1:g.27535910T>C	GRCh37
NC_000002.10:g.27389414T>C	NCBI36
NG_008075.1:g.14522A>G
NG_033055.1:g.221A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380044.6:c.137A>G MANE Select	ENSP00000369383.1:p.His46Arg
ENST00000233545.6:c.137A>G	ENSP00000233545.2:p.His46Arg
ENST00000357186.10:c.19-271A>G	ENSP00000349713.6:n.19-271A>G
ENST00000380044.5:c.137A>G	ENSP00000369383.1:p.His46Arg
ENST00000402310.5:c.137A>G	ENSP00000383955.1:p.His46Arg
ENST00000402722.5:c.102A>G	ENSP00000386000.1:p.Thr34=
ENST00000403262.6:c.137A>G	ENSP00000385671.1:p.His46Arg
ENST00000405076.5:c.137A>G	ENSP00000385175.1:p.His46Arg
ENST00000405983.5:c.182A>G	ENSP00000384586.1:p.His61Arg
ENST00000415514.5:c.228-271A>G	ENSP00000388043.1:n.228-271A>G
ENST00000426513.6:c.102A>G	ENSP00000403824.2:p.Thr34=
ENST00000428910.5:c.59A>G	ENSP00000405235.1:p.His20Arg
ENST00000430991.5:c.67A>G
ENST00000616446.1:n.114A>G
ENST00000616707.1:n.345A>G
ENST00000617583.4:n.163A>G
ENST00000621183.4:n.193A>G
ENST00000621470.4:n.153A>G
ENST00000622003.4:n.310A>G
NM_002437.4:c.137A>G	NP_002428.1:p.His46Arg
XM_005264326.2:c.137A>G	XP_005264383.1:p.His46Arg
XM_005264327.2:c.-23A>G	XP_005264384.1:n.-23A>G
XM_006712021.2:c.89A>G	XP_006712084.1:p.His30Arg
XM_005264326.4:c.137A>G	XP_005264383.1:p.His46Arg
XM_006712021.3:c.89A>G	XP_006712084.1:p.His30Arg
XM_017004150.1:c.119A>G	XP_016859639.1:p.His40Arg
XM_017004151.1:c.89A>G	XP_016859640.1:p.His30Arg
XM_017004152.1:c.-23A>G	XP_016859641.1:n.-23A>G
XM_024452913.1:c.89A>G	XP_024308681.1:p.His30Arg
NM_002437.5:c.137A>G MANE Select	NP_002428.1:p.His46Arg