Canonical Allele Identifier: CA1562859325
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692771T= , CM000667.2:g.90692771T= GRCh38
NC_000005.9:g.89988588T= , CM000667.1:g.89988588T= GRCh37
NC_000005.8:g.90024344T= NCBI36
NG_007083.1:g.138972T=
NG_007083.2:g.168428T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7118T= MANE Select ENSP00000384582.2:p.Ile2373=
ENST00000639431.1:c.265+16562T= ENSP00000491057.1:n.265+16562T=
ENST00000639473.1:n.2577T=
ENST00000640012.1:c.925T=
ENST00000640374.1:n.262T=
ENST00000640403.1:c.4409T= ENSP00000492531.1:p.Ile1470=
ENST00000640779.1:c.1847T=
ENST00000405460.6:c.7118T= ENSP00000384582.2:p.Ile2373=
NM_032119.3:c.7118T= NP_115495.3:p.Ile2373=
NR_003149.1:n.7131T=
XM_011543675.1:c.7115T= XP_011541977.1:p.Ile2372=
XM_011543676.1:c.7037T= XP_011541978.1:p.Ile2346=
XM_011543677.1:c.4421T= XP_011541979.1:p.Ile1474=
XM_011543678.1:c.7118T= XP_011541980.1:p.Ile2373=
XM_011543679.1:c.7118T= XP_011541981.1:p.Ile2373=
NM_032119.4:c.7118T= MANE Select NP_115495.3:p.Ile2373=
XM_017009963.2:c.7118T= XP_016865452.1:p.Ile2373=
XM_017009964.2:c.7115T= XP_016865453.1:p.Ile2372=
XM_017009965.1:c.7115T= XP_016865454.1:p.Ile2372=
XM_017009966.2:c.7037T= XP_016865455.1:p.Ile2346=
XM_017009967.1:c.7022T= XP_016865456.1:p.Ile2341=
XM_017009968.2:c.7118T= XP_016865457.1:p.Ile2373=
XM_017009969.2:c.7118T= XP_016865458.1:p.Ile2373=
XM_017009970.2:c.7118T= XP_016865459.1:p.Ile2373=
XM_017009971.2:c.7118T= XP_016865460.1:p.Ile2373=
XM_017009972.1:c.236T= XP_016865461.1:p.Ile79=
XM_017009973.1:c.236T= XP_016865462.1:p.Ile79=
XM_017009974.2:c.7118T= XP_016865463.1:p.Ile2373=
NR_003149.2:n.7134T=