Canonical Allele Identifier: CA3342287

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90848692A>G , CM000667.2:g.90848692A>G	GRCh38
NC_000005.9:g.90144509A>G , CM000667.1:g.90144509A>G	GRCh37
NC_000005.8:g.90180265A>G	NCBI36
NG_007083.1:g.294893A>G
NG_007083.2:g.324349A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17075A>G MANE Select	NP_115495.3:p.Tyr5692Cys
ENST00000405460.9:c.17075A>G MANE Select	ENSP00000384582.2:p.Tyr5692Cys
NM_032119.3:c.17075A>G	NP_115495.3:p.Tyr5692Cys
NR_003149.1:n.17088A>G
NR_003149.2:n.17091A>G
ENST00000405460.6:c.17075A>G	ENSP00000384582.2:p.Tyr5692Cys
ENST00000425867.2:c.4058A>G	ENSP00000392618.2:p.Tyr1353Cys
ENST00000425867.3:c.6029A>G	ENSP00000392618.3:p.Tyr2010Cys
ENST00000505845.1:n.266A>G
ENST00000505845.2:n.266A>G
ENST00000638510.1:n.4342A>G
ENST00000638990.1:c.96A>G
ENST00000639431.1:c.266-136652A>G	ENSP00000491057.1:n.266-136652A>G
ENST00000640407.1:c.3524A>G	ENSP00000491425.1:n.3524A>G
XM_011543675.1:c.17072A>G	XP_011541977.1:p.Tyr5691Cys
XM_011543676.1:c.16994A>G	XP_011541978.1:p.Tyr5665Cys
XM_011543677.1:c.14378A>G	XP_011541979.1:p.Tyr4793Cys
XM_017009963.2:c.17096A>G	XP_016865452.1:p.Tyr5699Cys
XM_017009964.2:c.17093A>G	XP_016865453.1:p.Tyr5698Cys
XM_017009965.1:c.17093A>G	XP_016865454.1:p.Tyr5698Cys
XM_017009966.2:c.17015A>G	XP_016865455.1:p.Tyr5672Cys
XM_017009967.1:c.17000A>G	XP_016865456.1:p.Tyr5667Cys
XM_017009968.2:c.16916A>G	XP_016865457.1:p.Tyr5639Cys
XM_017009969.2:c.17096A>G	XP_016865458.1:p.Tyr5699Cys
XM_017009972.1:c.10214A>G	XP_016865461.1:p.Tyr3405Cys
XM_017009973.1:c.10193A>G	XP_016865462.1:p.Tyr3398Cys