Canonical Allele Identifier: CA1240215689

Gene: MPV17

Linked Data

• dbSNP Id: rs1679346623

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309558dup , CM000664.2:g.27309558dup	GRCh38
NC_000002.11:g.27532426dup , CM000664.1:g.27532426dup	GRCh37
NC_000002.10:g.27385930dup	NCBI36
NG_008075.1:g.18008dup
NG_033055.1:g.3707dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.*356dup MANE Select	ENSP00000369383.1:n.*356dup
ENST00000233545.6:c.*356dup	ENSP00000233545.2:n.*356dup
ENST00000357186.10:c.*356dup	ENSP00000349713.6:n.*356dup
ENST00000380044.5:c.*356dup	ENSP00000369383.1:n.*356dup
ENST00000402310.5:c.*321dup	ENSP00000383955.1:n.*321dup
ENST00000402722.5:c.*466dup	ENSP00000386000.1:n.*466dup
ENST00000426513.6:c.*552dup	ENSP00000403824.2:n.*552dup
ENST00000620797.4:n.560dup
NM_002437.4:c.*356dup	NP_002428.1:n.*356dup
XM_005264326.2:c.*356dup	XP_005264383.1:n.*356dup
XM_005264327.2:c.*356dup	XP_005264384.1:n.*356dup
XM_006712021.2:c.*356dup	XP_006712084.1:n.*356dup
XM_005264326.4:c.*356dup	XP_005264383.1:n.*356dup
XM_006712021.3:c.*356dup	XP_006712084.1:n.*356dup
XM_017004150.1:c.*356dup	XP_016859639.1:n.*356dup
XM_017004151.1:c.*356dup	XP_016859640.1:n.*356dup
XM_017004152.1:c.*356dup	XP_016859641.1:n.*356dup
XM_024452913.1:c.*356dup	XP_024308681.1:n.*356dup
NM_002437.5:c.*356dup MANE Select	NP_002428.1:n.*356dup