Canonical Allele Identifier: CA2658325508

Gene: MPV17

Linked Data

• gnomAD v4: 2-27309875-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309876dup , CM000664.2:g.27309876dup	GRCh38
NC_000002.11:g.27532744dup , CM000664.1:g.27532744dup	GRCh37
NC_000002.10:g.27386248dup	NCBI36
NG_008075.1:g.17688dup
NG_033055.1:g.3387dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.*36dup MANE Select	ENSP00000369383.1:n.*36dup
ENST00000233545.6:c.*36dup	ENSP00000233545.2:n.*36dup
ENST00000357186.10:c.*36dup	ENSP00000349713.6:n.*36dup
ENST00000380044.5:c.*36dup	ENSP00000369383.1:n.*36dup
ENST00000402310.5:c.*1dup	ENSP00000383955.1:n.*1dup
ENST00000402722.5:c.*146dup	ENSP00000386000.1:n.*146dup
ENST00000405076.5:c.*36dup	ENSP00000385175.1:n.*36dup
ENST00000405983.5:c.*36dup	ENSP00000384586.1:n.*36dup
ENST00000426513.6:c.*232dup	ENSP00000403824.2:n.*232dup
ENST00000430991.5:c.401dup
ENST00000620797.4:n.240dup
ENST00000621183.4:n.870dup
NM_002437.4:c.*36dup	NP_002428.1:n.*36dup
XM_005264326.2:c.*36dup	XP_005264383.1:n.*36dup
XM_005264327.2:c.*36dup	XP_005264384.1:n.*36dup
XM_006712021.2:c.*36dup	XP_006712084.1:n.*36dup
XM_005264326.4:c.*36dup	XP_005264383.1:n.*36dup
XM_006712021.3:c.*36dup	XP_006712084.1:n.*36dup
XM_017004150.1:c.*36dup	XP_016859639.1:n.*36dup
XM_017004151.1:c.*36dup	XP_016859640.1:n.*36dup
XM_017004152.1:c.*36dup	XP_016859641.1:n.*36dup
XM_024452913.1:c.*36dup	XP_024308681.1:n.*36dup
NM_002437.5:c.*36dup MANE Select	NP_002428.1:n.*36dup