Canonical Allele Identifier: CA176212
Gene: ADGRV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 163593
dbSNP Id: rs727503078

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725561A>G , CM000667.2:g.90725561A>G GRCh38
NC_000005.9:g.90021378A>G , CM000667.1:g.90021378A>G GRCh37
NC_000005.8:g.90057134A>G NCBI36
NG_007083.1:g.171762A>G
NG_007083.2:g.201218A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10066A>G MANE Select ENSP00000384582.2:p.Ile3356Val
ENST00000639431.1:n.265+49352A>G ENSP00000491057.1:p.=
ENST00000640374.1:n.3210A>G
ENST00000640464.1:n.485A>G
ENST00000405460.6:c.10066A>G ENSP00000384582.2:p.Ile3356Val
ENST00000509621.1:n.2763A>G
NM_032119.3:c.10066A>G NP_115495.3:p.Ile3356Val
NR_003149.1:n.10079A>G
XM_011543675.1:c.10063A>G XP_011541977.1:p.Ile3355Val
XM_011543676.1:c.9985A>G XP_011541978.1:p.Ile3329Val
XM_011543677.1:c.7369A>G XP_011541979.1:p.Ile2457Val
XM_011543678.1:c.10066A>G XP_011541980.1:p.Ile3356Val
XM_011543679.1:c.10066A>G XP_011541981.1:p.Ile3356Val
XR_948560.1:n.272-9752T>C
NM_032119.4:c.10066A>G MANE Select NP_115495.3:p.Ile3356Val
XM_017009963.2:c.10087A>G XP_016865452.1:p.Ile3363Val
XM_017009964.2:c.10084A>G XP_016865453.1:p.Ile3362Val
XM_017009965.1:c.10084A>G XP_016865454.1:p.Ile3362Val
XM_017009966.2:c.10006A>G XP_016865455.1:p.Ile3336Val
XM_017009967.1:c.9991A>G XP_016865456.1:p.Ile3331Val
XM_017009968.2:c.10087A>G XP_016865457.1:p.Ile3363Val
XM_017009969.2:c.10087A>G XP_016865458.1:p.Ile3363Val
XM_017009970.2:c.10087A>G XP_016865459.1:p.Ile3363Val
XM_017009971.2:c.10087A>G XP_016865460.1:p.Ile3363Val
XM_017009972.1:c.3205A>G XP_016865461.1:p.Ile1069Val
XM_017009973.1:c.3184A>G XP_016865462.1:p.Ile1062Val
XM_017009974.2:c.10087A>G XP_016865463.1:p.Ile3363Val
XR_001742802.1:n.2523-9752T>C
NR_003149.2:n.10082A>G