Canonical Allele Identifier: CA346209092

Gene: MPV17

Linked Data

• gnomAD v4: 2-27312994-C-T
• MyVariant Identifiers: chr2:g.27535861C>T (hg19) ; chr2:g.27312994C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27312994C>T , CM000664.2:g.27312994C>T	GRCh38
NC_000002.11:g.27535861C>T , CM000664.1:g.27535861C>T	GRCh37
NC_000002.10:g.27389365C>T	NCBI36
NG_008075.1:g.14571G>A
NG_033055.1:g.270G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.186G>A MANE Select	ENSP00000369383.1:p.Val62=
ENST00000233545.6:c.186G>A	ENSP00000233545.2:p.Val62=
ENST00000357186.10:c.19-222G>A	ENSP00000349713.6:n.19-222G>A
ENST00000380044.5:c.186G>A	ENSP00000369383.1:p.Val62=
ENST00000402310.5:c.186G>A	ENSP00000383955.1:p.Val62=
ENST00000402722.5:c.151G>A	ENSP00000386000.1:p.Gly51Arg
ENST00000403262.6:c.186G>A	ENSP00000385671.1:p.Val62=
ENST00000405076.5:c.186G>A	ENSP00000385175.1:p.Val62=
ENST00000405983.5:c.231G>A	ENSP00000384586.1:p.Val77=
ENST00000415514.5:c.228-222G>A	ENSP00000388043.1:n.228-222G>A
ENST00000426513.6:c.151G>A	ENSP00000403824.2:p.Gly51Arg
ENST00000428910.5:c.108G>A	ENSP00000405235.1:p.Val36=
ENST00000430991.5:c.116G>A
ENST00000616446.1:n.163G>A
ENST00000616707.1:n.394G>A
ENST00000617583.4:n.212G>A
ENST00000621183.4:n.242G>A
ENST00000621470.4:n.202G>A
ENST00000622003.4:n.359G>A
NM_002437.4:c.186G>A	NP_002428.1:p.Val62=
XM_005264326.2:c.186G>A	XP_005264383.1:p.Val62=
XM_005264327.2:c.27G>A	XP_005264384.1:p.Val9=
XM_006712021.2:c.138G>A	XP_006712084.1:p.Val46=
XM_005264326.4:c.186G>A	XP_005264383.1:p.Val62=
XM_006712021.3:c.138G>A	XP_006712084.1:p.Val46=
XM_017004150.1:c.168G>A	XP_016859639.1:p.Val56=
XM_017004151.1:c.138G>A	XP_016859640.1:p.Val46=
XM_017004152.1:c.27G>A	XP_016859641.1:p.Val9=
XM_024452913.1:c.138G>A	XP_024308681.1:p.Val46=
NM_002437.5:c.186G>A MANE Select	NP_002428.1:p.Val62=