Canonical Allele Identifier: CA2576929079

Gene: MPV17

Linked Data

• ClinVar Variation Id: 2985747
• ClinVar RCV Id: RCV003841354

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27309995A>G , CM000664.2:g.27309995A>G	GRCh38
NC_000002.11:g.27532863A>G , CM000664.1:g.27532863A>G	GRCh37
NC_000002.10:g.27386367A>G	NCBI36
NG_008075.1:g.17569T>C
NG_033055.1:g.3268T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380044.6:c.462-14T>C MANE Select	ENSP00000369383.1:n.462-14T>C
ENST00000233545.6:c.462-14T>C	ENSP00000233545.2:n.462-14T>C
ENST00000357186.10:c.294-14T>C	ENSP00000349713.6:n.294-14T>C
ENST00000380044.5:c.462-14T>C	ENSP00000369383.1:n.462-14T>C
ENST00000402310.5:c.409-14T>C	ENSP00000383955.1:n.409-14T>C
ENST00000402722.5:c.*41-14T>C	ENSP00000386000.1:n.*41-14T>C
ENST00000405076.5:c.273-14T>C	ENSP00000385175.1:n.273-14T>C
ENST00000405983.5:c.507-14T>C	ENSP00000384586.1:n.507-14T>C
ENST00000415514.5:c.*263-14T>C	ENSP00000388043.1:n.*263-14T>C
ENST00000426513.6:c.*127-14T>C	ENSP00000403824.2:n.*127-14T>C
ENST00000430991.5:c.296-14T>C
ENST00000620797.4:n.135-14T>C
ENST00000621183.4:n.765-14T>C
NM_002437.4:c.462-14T>C	NP_002428.1:n.462-14T>C
XM_005264326.2:c.462-14T>C	XP_005264383.1:n.462-14T>C
XM_005264327.2:c.303-14T>C	XP_005264384.1:n.303-14T>C
XM_006712021.2:c.414-14T>C	XP_006712084.1:n.414-14T>C
XM_005264326.4:c.462-14T>C	XP_005264383.1:n.462-14T>C
XM_006712021.3:c.414-14T>C	XP_006712084.1:n.414-14T>C
XM_017004150.1:c.444-14T>C	XP_016859639.1:n.444-14T>C
XM_017004151.1:c.414-14T>C	XP_016859640.1:n.414-14T>C
XM_017004152.1:c.303-14T>C	XP_016859641.1:n.303-14T>C
XM_024452913.1:c.414-14T>C	XP_024308681.1:n.414-14T>C
NM_002437.5:c.462-14T>C MANE Select	NP_002428.1:n.462-14T>C