Canonical Allele Identifier: CA360414214
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90684063C>A , CM000667.2:g.90684063C>A GRCh38
NC_000005.9:g.89979880C>A , CM000667.1:g.89979880C>A GRCh37
NC_000005.8:g.90015636C>A NCBI36
NG_007083.1:g.130264C>A
NG_007083.2:g.159720C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.6142C>A MANE Select ENSP00000384582.2:p.Leu2048Ile
ENST00000639431.1:c.265+7854C>A ENSP00000491057.1:n.265+7854C>A
ENST00000639473.1:n.1601C>A
ENST00000640012.1:c.165-1717C>A
ENST00000640403.1:c.3433C>A ENSP00000492531.1:p.Leu1145Ile
ENST00000640779.1:c.954C>A
ENST00000405460.6:c.6142C>A ENSP00000384582.2:p.Leu2048Ile
NM_032119.3:c.6142C>A NP_115495.3:p.Leu2048Ile
NR_003149.1:n.6238C>A
XM_011543675.1:c.6139C>A XP_011541977.1:p.Leu2047Ile
XM_011543676.1:c.6061C>A XP_011541978.1:p.Leu2021Ile
XM_011543677.1:c.3445C>A XP_011541979.1:p.Leu1149Ile
XM_011543678.1:c.6142C>A XP_011541980.1:p.Leu2048Ile
XM_011543679.1:c.6142C>A XP_011541981.1:p.Leu2048Ile
NM_032119.4:c.6142C>A MANE Select NP_115495.3:p.Leu2048Ile
XM_017009963.2:c.6142C>A XP_016865452.1:p.Leu2048Ile
XM_017009964.2:c.6139C>A XP_016865453.1:p.Leu2047Ile
XM_017009965.1:c.6139C>A XP_016865454.1:p.Leu2047Ile
XM_017009966.2:c.6061C>A XP_016865455.1:p.Leu2021Ile
XM_017009967.1:c.6046C>A XP_016865456.1:p.Leu2016Ile
XM_017009968.2:c.6142C>A XP_016865457.1:p.Leu2048Ile
XM_017009969.2:c.6142C>A XP_016865458.1:p.Leu2048Ile
XM_017009970.2:c.6142C>A XP_016865459.1:p.Leu2048Ile
XM_017009971.2:c.6142C>A XP_016865460.1:p.Leu2048Ile
XM_017009973.1:c.-658C>A XP_016865462.1:n.-658C>A
XM_017009974.2:c.6142C>A XP_016865463.1:p.Leu2048Ile
NR_003149.2:n.6241C>A