Canonical Allele Identifier: CA360366265
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627377T>G , CM000667.2:g.90627377T>G GRCh38
NC_000005.9:g.89923194T>G , CM000667.1:g.89923194T>G GRCh37
NC_000005.8:g.89958950T>G NCBI36
NG_007083.1:g.73578T>G
NG_007083.2:g.103034T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.839T>G MANE Select ENSP00000384582.2:p.Ile280Arg
ENST00000640083.1:n.544T>G
ENST00000640109.1:n.935T>G
ENST00000640281.1:n.898T>G
ENST00000405460.6:c.839T>G ENSP00000384582.2:p.Ile280Arg
NM_032119.3:c.839T>G NP_115495.3:p.Ile280Arg
NR_003149.1:n.935T>G
XM_011543675.1:c.839T>G XP_011541977.1:p.Ile280Arg
XM_011543676.1:c.839T>G XP_011541978.1:p.Ile280Arg
XM_011543678.1:c.839T>G XP_011541980.1:p.Ile280Arg
XM_011543679.1:c.839T>G XP_011541981.1:p.Ile280Arg
NM_032119.4:c.839T>G MANE Select NP_115495.3:p.Ile280Arg
XM_017009963.2:c.839T>G XP_016865452.1:p.Ile280Arg
XM_017009964.2:c.839T>G XP_016865453.1:p.Ile280Arg
XM_017009965.1:c.836T>G XP_016865454.1:p.Ile279Arg
XM_017009966.2:c.839T>G XP_016865455.1:p.Ile280Arg
XM_017009967.1:c.743T>G XP_016865456.1:p.Ile248Arg
XM_017009968.2:c.839T>G XP_016865457.1:p.Ile280Arg
XM_017009969.2:c.839T>G XP_016865458.1:p.Ile280Arg
XM_017009970.2:c.839T>G XP_016865459.1:p.Ile280Arg
XM_017009971.2:c.839T>G XP_016865460.1:p.Ile280Arg
XM_017009974.2:c.839T>G XP_016865463.1:p.Ile280Arg
NR_003149.2:n.938T>G