Canonical Allele Identifier: CA346205398

Gene: MPV17

Linked Data

• MyVariant Identifiers: chr2:g.27532817C>T (hg19) ; chr2:g.27309949C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309949C>T , CM000664.2:g.27309949C>T	GRCh38
NC_000002.11:g.27532817C>T , CM000664.1:g.27532817C>T	GRCh37
NC_000002.10:g.27386321C>T	NCBI36
NG_008075.1:g.17615G>A
NG_033055.1:g.3314G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.494G>A MANE Select	ENSP00000369383.1:p.Trp165Ter
ENST00000233545.6:c.494G>A	ENSP00000233545.2:p.Trp165Ter
ENST00000357186.10:c.326G>A	ENSP00000349713.6:p.Trp109Ter
ENST00000380044.5:c.494G>A	ENSP00000369383.1:p.Trp165Ter
ENST00000402310.5:c.441G>A	ENSP00000383955.1:p.Leu147=
ENST00000402722.5:c.*73G>A	ENSP00000386000.1:n.*73G>A
ENST00000405076.5:c.305G>A	ENSP00000385175.1:p.Trp102Ter
ENST00000405983.5:c.539G>A	ENSP00000384586.1:p.Trp180Ter
ENST00000415514.5:c.*295G>A	ENSP00000388043.1:n.*295G>A
ENST00000426513.6:c.*159G>A	ENSP00000403824.2:n.*159G>A
ENST00000430991.5:c.328G>A
ENST00000620797.4:n.167G>A
ENST00000621183.4:n.797G>A
NM_002437.4:c.494G>A	NP_002428.1:p.Trp165Ter
XM_005264326.2:c.494G>A	XP_005264383.1:p.Trp165Ter
XM_005264327.2:c.335G>A	XP_005264384.1:p.Trp112Ter
XM_006712021.2:c.446G>A	XP_006712084.1:p.Trp149Ter
XM_005264326.4:c.494G>A	XP_005264383.1:p.Trp165Ter
XM_006712021.3:c.446G>A	XP_006712084.1:p.Trp149Ter
XM_017004150.1:c.476G>A	XP_016859639.1:p.Trp159Ter
XM_017004151.1:c.446G>A	XP_016859640.1:p.Trp149Ter
XM_017004152.1:c.335G>A	XP_016859641.1:p.Trp112Ter
XM_024452913.1:c.446G>A	XP_024308681.1:p.Trp149Ter
NM_002437.5:c.494G>A MANE Select	NP_002428.1:p.Trp165Ter