Canonical Allele Identifier: CA346208458

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27535552C>A (hg19) ; chr2:g.27312685C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312685C>A , CM000664.2:g.27312685C>A	GRCh38
NC_000002.11:g.27535552C>A , CM000664.1:g.27535552C>A	GRCh37
NC_000002.10:g.27389056C>A	NCBI36
NG_008075.1:g.14880G>T
NG_033055.1:g.579G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.274G>T MANE Select	ENSP00000369383.1:p.Asp92Tyr
ENST00000233545.6:c.274G>T	ENSP00000233545.2:p.Asp92Tyr
ENST00000357186.10:c.106G>T	ENSP00000349713.6:p.Asp36Tyr
ENST00000380044.5:c.274G>T	ENSP00000369383.1:p.Asp92Tyr
ENST00000402310.5:c.274G>T	ENSP00000383955.1:p.Asp92Tyr
ENST00000402722.5:c.239G>T	ENSP00000386000.1:p.Gly80Val
ENST00000403262.6:c.274G>T	ENSP00000385671.1:p.Asp92Tyr
ENST00000405076.5:c.186+309G>T	ENSP00000385175.1:n.186+309G>T
ENST00000405983.5:c.319G>T	ENSP00000384586.1:p.Asp107Tyr
ENST00000415514.5:c.*75G>T	ENSP00000388043.1:n.*75G>T
ENST00000426513.6:c.239G>T	ENSP00000403824.2:p.Gly80Val
ENST00000428910.5:c.196G>T	ENSP00000405235.1:p.Asp66Tyr
ENST00000430991.5:c.204G>T
ENST00000475085.1:n.302G>T
ENST00000616446.1:n.251G>T
ENST00000616707.1:n.703G>T
ENST00000617583.4:n.300G>T
ENST00000621183.4:n.330G>T
ENST00000621470.4:n.290G>T
ENST00000622003.4:n.447G>T
NM_002437.4:c.274G>T	NP_002428.1:p.Asp92Tyr
XM_005264326.2:c.274G>T	XP_005264383.1:p.Asp92Tyr
XM_005264327.2:c.115G>T	XP_005264384.1:p.Asp39Tyr
XM_006712021.2:c.226G>T	XP_006712084.1:p.Asp76Tyr
XM_005264326.4:c.274G>T	XP_005264383.1:p.Asp92Tyr
XM_006712021.3:c.226G>T	XP_006712084.1:p.Asp76Tyr
XM_017004150.1:c.256G>T	XP_016859639.1:p.Asp86Tyr
XM_017004151.1:c.226G>T	XP_016859640.1:p.Asp76Tyr
XM_017004152.1:c.115G>T	XP_016859641.1:p.Asp39Tyr
XM_024452913.1:c.226G>T	XP_024308681.1:p.Asp76Tyr
NM_002437.5:c.274G>T MANE Select	NP_002428.1:p.Asp92Tyr