Canonical Allele Identifier: CA360371458
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692707G>C , CM000667.2:g.90692707G>C GRCh38
NC_000005.9:g.89988524G>C , CM000667.1:g.89988524G>C GRCh37
NC_000005.8:g.90024280G>C NCBI36
NG_007083.1:g.138908G>C
NG_007083.2:g.168364G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7054G>C MANE Select ENSP00000384582.2:p.Val2352Leu
ENST00000639431.1:c.265+16498G>C ENSP00000491057.1:n.265+16498G>C
ENST00000639473.1:n.2513G>C
ENST00000640012.1:c.861G>C
ENST00000640374.1:n.198G>C
ENST00000640403.1:c.4345G>C ENSP00000492531.1:p.Val1449Leu
ENST00000640779.1:c.1783G>C
ENST00000405460.6:c.7054G>C ENSP00000384582.2:p.Val2352Leu
NM_032119.3:c.7054G>C NP_115495.3:p.Val2352Leu
NR_003149.1:n.7067G>C
XM_011543675.1:c.7051G>C XP_011541977.1:p.Val2351Leu
XM_011543676.1:c.6973G>C XP_011541978.1:p.Val2325Leu
XM_011543677.1:c.4357G>C XP_011541979.1:p.Val1453Leu
XM_011543678.1:c.7054G>C XP_011541980.1:p.Val2352Leu
XM_011543679.1:c.7054G>C XP_011541981.1:p.Val2352Leu
NM_032119.4:c.7054G>C MANE Select NP_115495.3:p.Val2352Leu
XM_017009963.2:c.7054G>C XP_016865452.1:p.Val2352Leu
XM_017009964.2:c.7051G>C XP_016865453.1:p.Val2351Leu
XM_017009965.1:c.7051G>C XP_016865454.1:p.Val2351Leu
XM_017009966.2:c.6973G>C XP_016865455.1:p.Val2325Leu
XM_017009967.1:c.6958G>C XP_016865456.1:p.Val2320Leu
XM_017009968.2:c.7054G>C XP_016865457.1:p.Val2352Leu
XM_017009969.2:c.7054G>C XP_016865458.1:p.Val2352Leu
XM_017009970.2:c.7054G>C XP_016865459.1:p.Val2352Leu
XM_017009971.2:c.7054G>C XP_016865460.1:p.Val2352Leu
XM_017009972.1:c.172G>C XP_016865461.1:p.Val58Leu
XM_017009973.1:c.172G>C XP_016865462.1:p.Val58Leu
XM_017009974.2:c.7054G>C XP_016865463.1:p.Val2352Leu
NR_003149.2:n.7070G>C