Canonical Allele Identifier: CA3339629

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90681448A>G , CM000667.2:g.90681448A>G	GRCh38
NC_000005.9:g.89977265A>G , CM000667.1:g.89977265A>G	GRCh37
NC_000005.8:g.90013021A>G	NCBI36
NG_007083.1:g.127649A>G
NG_007083.2:g.157105A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5658A>G MANE Select	NP_115495.3:p.Thr1886=
ENST00000405460.9:c.5658A>G MANE Select	ENSP00000384582.2:p.Thr1886=
NM_032119.3:c.5658A>G	NP_115495.3:p.Thr1886=
NR_003149.1:n.5754A>G
NR_003149.2:n.5757A>G
ENST00000405460.6:c.5658A>G	ENSP00000384582.2:p.Thr1886=
ENST00000639431.1:c.265+5239A>G	ENSP00000491057.1:n.265+5239A>G
ENST00000639473.1:n.1117A>G
ENST00000640012.1:c.158A>G
ENST00000640403.1:c.2949A>G	ENSP00000492531.1:p.Thr983=
ENST00000640779.1:c.470A>G
XM_011543675.1:c.5655A>G	XP_011541977.1:p.Thr1885=
XM_011543676.1:c.5577A>G	XP_011541978.1:p.Thr1859=
XM_011543677.1:c.2961A>G	XP_011541979.1:p.Thr987=
XM_011543678.1:c.5658A>G	XP_011541980.1:p.Thr1886=
XM_011543679.1:c.5658A>G	XP_011541981.1:p.Thr1886=
XM_017009963.2:c.5658A>G	XP_016865452.1:p.Thr1886=
XM_017009964.2:c.5655A>G	XP_016865453.1:p.Thr1885=
XM_017009965.1:c.5655A>G	XP_016865454.1:p.Thr1885=
XM_017009966.2:c.5577A>G	XP_016865455.1:p.Thr1859=
XM_017009967.1:c.5562A>G	XP_016865456.1:p.Thr1854=
XM_017009968.2:c.5658A>G	XP_016865457.1:p.Thr1886=
XM_017009969.2:c.5658A>G	XP_016865458.1:p.Thr1886=
XM_017009970.2:c.5658A>G	XP_016865459.1:p.Thr1886=
XM_017009971.2:c.5658A>G	XP_016865460.1:p.Thr1886=
XM_017009973.1:c.-1142A>G	XP_016865462.1:n.-1142A>G
XM_017009974.2:c.5658A>G	XP_016865463.1:p.Thr1886=