Canonical Allele Identifier: CA346209338

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535909G>A (hg19) ; chr2:g.27313042G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27313042G>A , CM000664.2:g.27313042G>A	GRCh38
NC_000002.11:g.27535909G>A , CM000664.1:g.27535909G>A	GRCh37
NC_000002.10:g.27389413G>A	NCBI36
NG_008075.1:g.14523C>T
NG_033055.1:g.222C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.138C>T MANE Select	ENSP00000369383.1:p.His46=
ENST00000233545.6:c.138C>T	ENSP00000233545.2:p.His46=
ENST00000357186.10:c.19-270C>T	ENSP00000349713.6:n.19-270C>T
ENST00000380044.5:c.138C>T	ENSP00000369383.1:p.His46=
ENST00000402310.5:c.138C>T	ENSP00000383955.1:p.His46=
ENST00000402722.5:c.103C>T	ENSP00000386000.1:p.Pro35Ser
ENST00000403262.6:c.138C>T	ENSP00000385671.1:p.His46=
ENST00000405076.5:c.138C>T	ENSP00000385175.1:p.His46=
ENST00000405983.5:c.183C>T	ENSP00000384586.1:p.His61=
ENST00000415514.5:c.228-270C>T	ENSP00000388043.1:n.228-270C>T
ENST00000426513.6:c.103C>T	ENSP00000403824.2:p.Pro35Ser
ENST00000428910.5:c.60C>T	ENSP00000405235.1:p.His20=
ENST00000430991.5:c.68C>T
ENST00000616446.1:n.115C>T
ENST00000616707.1:n.346C>T
ENST00000617583.4:n.164C>T
ENST00000621183.4:n.194C>T
ENST00000621470.4:n.154C>T
ENST00000622003.4:n.311C>T
NM_002437.4:c.138C>T	NP_002428.1:p.His46=
XM_005264326.2:c.138C>T	XP_005264383.1:p.His46=
XM_005264327.2:c.-22C>T	XP_005264384.1:n.-22C>T
XM_006712021.2:c.90C>T	XP_006712084.1:p.His30=
XM_005264326.4:c.138C>T	XP_005264383.1:p.His46=
XM_006712021.3:c.90C>T	XP_006712084.1:p.His30=
XM_017004150.1:c.120C>T	XP_016859639.1:p.His40=
XM_017004151.1:c.90C>T	XP_016859640.1:p.His30=
XM_017004152.1:c.-22C>T	XP_016859641.1:n.-22C>T
XM_024452913.1:c.90C>T	XP_024308681.1:p.His30=
NM_002437.5:c.138C>T MANE Select	NP_002428.1:p.His46=