Canonical Allele Identifier: CA1240215930
Gene: MPV17 HGNC NCBI

Linked Data

dbSNP Id: rs1679373094
gnomAD v4: 2-27310089-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27310089A>G , CM000664.2:g.27310089A>G GRCh38
NC_000002.11:g.27532957A>G , CM000664.1:g.27532957A>G GRCh37
NC_000002.10:g.27386461A>G NCBI36
NG_008075.1:g.17475T>C
NG_033055.1:g.3174T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000380044.6:c.462-108T>C MANE Select ENSP00000369383.1:n.462-108T>C
ENST00000233545.6:c.462-108T>C ENSP00000233545.2:n.462-108T>C
ENST00000357186.10:c.294-108T>C ENSP00000349713.6:n.294-108T>C
ENST00000380044.5:c.462-108T>C ENSP00000369383.1:n.462-108T>C
ENST00000402310.5:c.409-108T>C ENSP00000383955.1:n.409-108T>C
ENST00000402722.5:c.*41-108T>C ENSP00000386000.1:n.*41-108T>C
ENST00000405076.5:c.273-108T>C ENSP00000385175.1:n.273-108T>C
ENST00000405983.5:c.507-108T>C ENSP00000384586.1:n.507-108T>C
ENST00000415514.5:c.*263-108T>C ENSP00000388043.1:n.*263-108T>C
ENST00000426513.6:c.*127-108T>C ENSP00000403824.2:n.*127-108T>C
ENST00000430991.5:c.296-108T>C
ENST00000620797.4:n.135-108T>C
ENST00000621183.4:n.765-108T>C
NM_002437.4:c.462-108T>C NP_002428.1:n.462-108T>C
XM_005264326.2:c.462-108T>C XP_005264383.1:n.462-108T>C
XM_005264327.2:c.303-108T>C XP_005264384.1:n.303-108T>C
XM_006712021.2:c.414-108T>C XP_006712084.1:n.414-108T>C
XM_005264326.4:c.462-108T>C XP_005264383.1:n.462-108T>C
XM_006712021.3:c.414-108T>C XP_006712084.1:n.414-108T>C
XM_017004150.1:c.444-108T>C XP_016859639.1:n.444-108T>C
XM_017004151.1:c.414-108T>C XP_016859640.1:n.414-108T>C
XM_017004152.1:c.303-108T>C XP_016859641.1:n.303-108T>C
XM_024452913.1:c.414-108T>C XP_024308681.1:n.414-108T>C
NM_002437.5:c.462-108T>C MANE Select NP_002428.1:n.462-108T>C