Canonical Allele Identifier: CA2573134426

Gene: MPV17

Linked Data

• ClinVar Variation Id: 1621917
• ClinVar RCV Id: RCV002101962
• dbSNP Id: rs2148212315

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309987del , CM000664.2:g.27309987del	GRCh38
NC_000002.11:g.27532855del , CM000664.1:g.27532855del	GRCh37
NC_000002.10:g.27386359del	NCBI36
NG_008075.1:g.17578del
NG_033055.1:g.3277del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.462-5del MANE Select	ENSP00000369383.1:n.462-5del
ENST00000233545.6:c.462-5del	ENSP00000233545.2:n.462-5del
ENST00000357186.10:c.294-5del	ENSP00000349713.6:n.294-5del
ENST00000380044.5:c.462-5del	ENSP00000369383.1:n.462-5del
ENST00000402310.5:c.409-5del	ENSP00000383955.1:n.409-5del
ENST00000402722.5:c.*41-5del	ENSP00000386000.1:n.*41-5del
ENST00000405076.5:c.273-5del	ENSP00000385175.1:n.273-5del
ENST00000405983.5:c.507-5del	ENSP00000384586.1:n.507-5del
ENST00000415514.5:c.*263-5del	ENSP00000388043.1:n.*263-5del
ENST00000426513.6:c.*127-5del	ENSP00000403824.2:n.*127-5del
ENST00000430991.5:c.296-5del
ENST00000620797.4:n.135-5del
ENST00000621183.4:n.765-5del
NM_002437.4:c.462-5del	NP_002428.1:n.462-5del
XM_005264326.2:c.462-5del	XP_005264383.1:n.462-5del
XM_005264327.2:c.303-5del	XP_005264384.1:n.303-5del
XM_006712021.2:c.414-5del	XP_006712084.1:n.414-5del
XM_005264326.4:c.462-5del	XP_005264383.1:n.462-5del
XM_006712021.3:c.414-5del	XP_006712084.1:n.414-5del
XM_017004150.1:c.444-5del	XP_016859639.1:n.444-5del
XM_017004151.1:c.414-5del	XP_016859640.1:n.414-5del
XM_017004152.1:c.303-5del	XP_016859641.1:n.303-5del
XM_024452913.1:c.414-5del	XP_024308681.1:n.414-5del
NM_002437.5:c.462-5del MANE Select	NP_002428.1:n.462-5del