Canonical Allele Identifier: CA346208164
Gene: MPV17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27312560G>T , CM000664.2:g.27312560G>T GRCh38
NC_000002.11:g.27535427G>T , CM000664.1:g.27535427G>T GRCh37
NC_000002.10:g.27388931G>T NCBI36
NG_008075.1:g.15005C>A
NG_033055.1:g.704C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.309C>A MANE Select ENSP00000369383.1:p.Cys103Ter
ENST00000233545.6:c.309C>A ENSP00000233545.2:p.Cys103Ter
ENST00000357186.10:c.141C>A ENSP00000349713.6:p.Cys47Ter
ENST00000380044.5:c.309C>A ENSP00000369383.1:p.Cys103Ter
ENST00000402310.5:c.309C>A ENSP00000383955.1:p.Cys103Ter
ENST00000402722.5:c.274C>A ENSP00000386000.1:p.Leu92Ile
ENST00000403262.6:c.309C>A ENSP00000385671.1:p.Cys103Ter
ENST00000405076.5:c.187-314C>A ENSP00000385175.1:n.187-314C>A
ENST00000405983.5:c.354C>A ENSP00000384586.1:p.Cys118Ter
ENST00000415514.5:c.*110C>A ENSP00000388043.1:n.*110C>A
ENST00000426513.6:c.274C>A ENSP00000403824.2:p.Leu92Ile
ENST00000428910.5:c.231C>A ENSP00000405235.1:p.Cys77Ter
ENST00000430991.5:c.209+120C>A
ENST00000475085.1:n.337C>A
ENST00000616446.1:n.286C>A
ENST00000616707.1:n.828C>A
ENST00000617583.4:n.335C>A
ENST00000621183.4:n.365C>A
ENST00000621470.4:n.325C>A
ENST00000622003.4:n.482C>A
NM_002437.4:c.309C>A NP_002428.1:p.Cys103Ter
XM_005264326.2:c.309C>A XP_005264383.1:p.Cys103Ter
XM_005264327.2:c.150C>A XP_005264384.1:p.Cys50Ter
XM_006712021.2:c.261C>A XP_006712084.1:p.Cys87Ter
XM_005264326.4:c.309C>A XP_005264383.1:p.Cys103Ter
XM_006712021.3:c.261C>A XP_006712084.1:p.Cys87Ter
XM_017004150.1:c.291C>A XP_016859639.1:p.Cys97Ter
XM_017004151.1:c.261C>A XP_016859640.1:p.Cys87Ter
XM_017004152.1:c.150C>A XP_016859641.1:p.Cys50Ter
XM_024452913.1:c.261C>A XP_024308681.1:p.Cys87Ter
NM_002437.5:c.309C>A MANE Select NP_002428.1:p.Cys103Ter