Canonical Allele Identifier: CA3340150

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90697025T>G , CM000667.2:g.90697025T>G	GRCh38
NC_000005.9:g.89992842T>G , CM000667.1:g.89992842T>G	GRCh37
NC_000005.8:g.90028598T>G	NCBI36
NG_007083.1:g.143226T>G
NG_007083.2:g.172682T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8034T>G MANE Select	NP_115495.3:p.Thr2678=
ENST00000405460.9:c.8034T>G MANE Select	ENSP00000384582.2:p.Thr2678=
NM_032119.3:c.8034T>G	NP_115495.3:p.Thr2678=
NR_003149.1:n.8047T>G
NR_003149.2:n.8050T>G
ENST00000405460.6:c.8034T>G	ENSP00000384582.2:p.Thr2678=
ENST00000509621.1:c.731T>G
ENST00000639431.1:c.265+20816T>G	ENSP00000491057.1:n.265+20816T>G
ENST00000639473.1:n.3493T>G
ENST00000640012.1:c.1841T>G
ENST00000640374.1:n.1178T>G
ENST00000640403.1:c.5325T>G	ENSP00000492531.1:p.Thr1775=
ENST00000640779.1:c.2763T>G
XM_011543675.1:c.8031T>G	XP_011541977.1:p.Thr2677=
XM_011543676.1:c.7953T>G	XP_011541978.1:p.Thr2651=
XM_011543677.1:c.5337T>G	XP_011541979.1:p.Thr1779=
XM_011543678.1:c.8034T>G	XP_011541980.1:p.Thr2678=
XM_011543679.1:c.8034T>G	XP_011541981.1:p.Thr2678=
XM_017009963.2:c.8034T>G	XP_016865452.1:p.Thr2678=
XM_017009964.2:c.8031T>G	XP_016865453.1:p.Thr2677=
XM_017009965.1:c.8031T>G	XP_016865454.1:p.Thr2677=
XM_017009966.2:c.7953T>G	XP_016865455.1:p.Thr2651=
XM_017009967.1:c.7938T>G	XP_016865456.1:p.Thr2646=
XM_017009968.2:c.8034T>G	XP_016865457.1:p.Thr2678=
XM_017009969.2:c.8034T>G	XP_016865458.1:p.Thr2678=
XM_017009970.2:c.8034T>G	XP_016865459.1:p.Thr2678=
XM_017009971.2:c.8034T>G	XP_016865460.1:p.Thr2678=
XM_017009972.1:c.1152T>G	XP_016865461.1:p.Thr384=
XM_017009973.1:c.1152T>G	XP_016865462.1:p.Thr384=
XM_017009974.2:c.8034T>G	XP_016865463.1:p.Thr2678=