Canonical Allele Identifier: CA3340599

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90724903A>G , CM000667.2:g.90724903A>G	GRCh38
NC_000005.9:g.90020720A>G , CM000667.1:g.90020720A>G	GRCh37
NC_000005.8:g.90056476A>G	NCBI36
NG_007083.1:g.171104A>G
NG_007083.2:g.200560A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9820A>G MANE Select	NP_115495.3:p.Thr3274Ala
ENST00000405460.9:c.9820A>G MANE Select	ENSP00000384582.2:p.Thr3274Ala
NM_032119.3:c.9820A>G	NP_115495.3:p.Thr3274Ala
NR_003149.1:n.9833A>G
NR_003149.2:n.9836A>G
ENST00000405460.6:c.9820A>G	ENSP00000384582.2:p.Thr3274Ala
ENST00000509621.1:c.2517A>G
ENST00000639431.1:c.265+48694A>G	ENSP00000491057.1:n.265+48694A>G
ENST00000640374.1:n.2964A>G
ENST00000640464.1:n.239A>G
ENST00000640779.1:c.4549A>G
XM_011543675.1:c.9817A>G	XP_011541977.1:p.Thr3273Ala
XM_011543676.1:c.9739A>G	XP_011541978.1:p.Thr3247Ala
XM_011543677.1:c.7123A>G	XP_011541979.1:p.Thr2375Ala
XM_011543678.1:c.9820A>G	XP_011541980.1:p.Thr3274Ala
XM_011543679.1:c.9820A>G	XP_011541981.1:p.Thr3274Ala
XM_017009963.2:c.9841A>G	XP_016865452.1:p.Thr3281Ala
XM_017009964.2:c.9838A>G	XP_016865453.1:p.Thr3280Ala
XM_017009965.1:c.9838A>G	XP_016865454.1:p.Thr3280Ala
XM_017009966.2:c.9760A>G	XP_016865455.1:p.Thr3254Ala
XM_017009967.1:c.9745A>G	XP_016865456.1:p.Thr3249Ala
XM_017009968.2:c.9841A>G	XP_016865457.1:p.Thr3281Ala
XM_017009969.2:c.9841A>G	XP_016865458.1:p.Thr3281Ala
XM_017009970.2:c.9841A>G	XP_016865459.1:p.Thr3281Ala
XM_017009971.2:c.9841A>G	XP_016865460.1:p.Thr3281Ala
XM_017009972.1:c.2959A>G	XP_016865461.1:p.Thr987Ala
XM_017009973.1:c.2938A>G	XP_016865462.1:p.Thr980Ala
XM_017009974.2:c.9841A>G	XP_016865463.1:p.Thr3281Ala
XR_001742802.1:n.2523-9094T>C
XR_948560.1:n.272-9094T>C