Canonical Allele Identifier: CA346207900

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535384C>A (hg19) ; chr2:g.27312517C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312517C>A , CM000664.2:g.27312517C>A	GRCh38
NC_000002.11:g.27535384C>A , CM000664.1:g.27535384C>A	GRCh37
NC_000002.10:g.27388888C>A	NCBI36
NG_008075.1:g.15048G>T
NG_033055.1:g.747G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.352G>T MANE Select	ENSP00000369383.1:p.Asp118Tyr
ENST00000233545.6:c.352G>T	ENSP00000233545.2:p.Asp118Tyr
ENST00000357186.10:c.184G>T	ENSP00000349713.6:p.Asp62Tyr
ENST00000380044.5:c.352G>T	ENSP00000369383.1:p.Asp118Tyr
ENST00000402310.5:c.352G>T	ENSP00000383955.1:p.Asp118Tyr
ENST00000402722.5:c.*17G>T	ENSP00000386000.1:n.*17G>T
ENST00000403262.6:c.352G>T	ENSP00000385671.1:p.Asp118Tyr
ENST00000405076.5:c.187-271G>T	ENSP00000385175.1:n.187-271G>T
ENST00000405983.5:c.397G>T	ENSP00000384586.1:p.Asp133Tyr
ENST00000415514.5:c.*153G>T	ENSP00000388043.1:n.*153G>T
ENST00000426513.6:c.*17G>T	ENSP00000403824.2:n.*17G>T
ENST00000428910.5:c.274G>T	ENSP00000405235.1:p.Asp92Tyr
ENST00000430991.5:c.209+163G>T
ENST00000475085.1:n.380G>T
ENST00000616446.1:n.329G>T
ENST00000616707.1:n.871G>T
ENST00000617583.4:n.378G>T
ENST00000621183.4:n.408G>T
ENST00000621470.4:n.368G>T
ENST00000622003.4:n.525G>T
NM_002437.4:c.352G>T	NP_002428.1:p.Asp118Tyr
XM_005264326.2:c.352G>T	XP_005264383.1:p.Asp118Tyr
XM_005264327.2:c.193G>T	XP_005264384.1:p.Asp65Tyr
XM_006712021.2:c.304G>T	XP_006712084.1:p.Asp102Tyr
XM_005264326.4:c.352G>T	XP_005264383.1:p.Asp118Tyr
XM_006712021.3:c.304G>T	XP_006712084.1:p.Asp102Tyr
XM_017004150.1:c.334G>T	XP_016859639.1:p.Asp112Tyr
XM_017004151.1:c.304G>T	XP_016859640.1:p.Asp102Tyr
XM_017004152.1:c.193G>T	XP_016859641.1:p.Asp65Tyr
XM_024452913.1:c.304G>T	XP_024308681.1:p.Asp102Tyr
NM_002437.5:c.352G>T MANE Select	NP_002428.1:p.Asp118Tyr