Canonical Allele Identifier: CA3341706

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791148A>G , CM000667.2:g.90791148A>G	GRCh38
NC_000005.9:g.90086965A>G , CM000667.1:g.90086965A>G	GRCh37
NC_000005.8:g.90122721A>G	NCBI36
NG_007083.1:g.237349A>G
NG_007083.2:g.266805A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14319A>G MANE Select	NP_115495.3:p.Ile4773Met
ENST00000405460.9:c.14319A>G MANE Select	ENSP00000384582.2:p.Ile4773Met
NM_032119.3:c.14319A>G	NP_115495.3:p.Ile4773Met
NR_003149.1:n.14332A>G
NR_003149.2:n.14335A>G
ENST00000405460.6:c.14319A>G	ENSP00000384582.2:p.Ile4773Met
ENST00000425867.2:c.1302A>G	ENSP00000392618.2:p.Ile434Met
ENST00000425867.3:c.3273A>G	ENSP00000392618.3:p.Ile1091Met
ENST00000638510.1:n.1586A>G
ENST00000638585.1:n.85A>G
ENST00000638975.1:c.948A>G	ENSP00000492630.1:p.Ile316Met
ENST00000639431.1:c.265+114939A>G	ENSP00000491057.1:n.265+114939A>G
ENST00000640407.1:c.729A>G	ENSP00000491425.1:p.Ile243Met
XM_011543675.1:c.14316A>G	XP_011541977.1:p.Ile4772Met
XM_011543676.1:c.14238A>G	XP_011541978.1:p.Ile4746Met
XM_011543677.1:c.11622A>G	XP_011541979.1:p.Ile3874Met
XM_011543678.1:c.14319A>G	XP_011541980.1:p.Ile4773Met
XM_017009963.2:c.14340A>G	XP_016865452.1:p.Ile4780Met
XM_017009964.2:c.14337A>G	XP_016865453.1:p.Ile4779Met
XM_017009965.1:c.14337A>G	XP_016865454.1:p.Ile4779Met
XM_017009966.2:c.14259A>G	XP_016865455.1:p.Ile4753Met
XM_017009967.1:c.14244A>G	XP_016865456.1:p.Ile4748Met
XM_017009968.2:c.14340A>G	XP_016865457.1:p.Ile4780Met
XM_017009969.2:c.14340A>G	XP_016865458.1:p.Ile4780Met
XM_017009970.2:c.14340A>G	XP_016865459.1:p.Ile4780Met
XM_017009971.2:c.14340A>G	XP_016865460.1:p.Ile4780Met
XM_017009972.1:c.7458A>G	XP_016865461.1:p.Ile2486Met
XM_017009973.1:c.7437A>G	XP_016865462.1:p.Ile2479Met