Canonical Allele Identifier: CA3341165

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763360C>T , CM000667.2:g.90763360C>T	GRCh38
NC_000005.9:g.90059177C>T , CM000667.1:g.90059177C>T	GRCh37
NC_000005.8:g.90094933C>T	NCBI36
NG_007083.1:g.209561C>T
NG_007083.2:g.239017C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12176C>T MANE Select	NP_115495.3:p.Thr4059Met
ENST00000405460.9:c.12176C>T MANE Select	ENSP00000384582.2:p.Thr4059Met
NM_032119.3:c.12176C>T	NP_115495.3:p.Thr4059Met
NR_003149.1:n.12189C>T
NR_003149.2:n.12192C>T
ENST00000405460.6:c.12176C>T	ENSP00000384582.2:p.Thr4059Met
ENST00000425867.3:c.1130C>T	ENSP00000392618.3:p.Thr377Met
ENST00000639431.1:c.265+87151C>T	ENSP00000491057.1:n.265+87151C>T
ENST00000640464.1:n.2595C>T
ENST00000640729.1:n.753C>T
XM_011543675.1:c.12173C>T	XP_011541977.1:p.Thr4058Met
XM_011543676.1:c.12095C>T	XP_011541978.1:p.Thr4032Met
XM_011543677.1:c.9479C>T	XP_011541979.1:p.Thr3160Met
XM_011543678.1:c.12176C>T	XP_011541980.1:p.Thr4059Met
XM_017009963.2:c.12197C>T	XP_016865452.1:p.Thr4066Met
XM_017009964.2:c.12194C>T	XP_016865453.1:p.Thr4065Met
XM_017009965.1:c.12194C>T	XP_016865454.1:p.Thr4065Met
XM_017009966.2:c.12116C>T	XP_016865455.1:p.Thr4039Met
XM_017009967.1:c.12101C>T	XP_016865456.1:p.Thr4034Met
XM_017009968.2:c.12197C>T	XP_016865457.1:p.Thr4066Met
XM_017009969.2:c.12197C>T	XP_016865458.1:p.Thr4066Met
XM_017009970.2:c.12197C>T	XP_016865459.1:p.Thr4066Met
XM_017009971.2:c.12197C>T	XP_016865460.1:p.Thr4066Met
XM_017009972.1:c.5315C>T	XP_016865461.1:p.Thr1772Met
XM_017009973.1:c.5294C>T	XP_016865462.1:p.Thr1765Met