Canonical Allele Identifier: CA3342339

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90853355A>G , CM000667.2:g.90853355A>G	GRCh38
NC_000005.9:g.90149172A>G , CM000667.1:g.90149172A>G	GRCh37
NC_000005.8:g.90184928A>G	NCBI36
NG_007083.1:g.299556A>G
NG_007083.2:g.329012A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17276A>G MANE Select	NP_115495.3:p.Asn5759Ser
ENST00000405460.9:c.17276A>G MANE Select	ENSP00000384582.2:p.Asn5759Ser
NM_032119.3:c.17276A>G	NP_115495.3:p.Asn5759Ser
NR_003149.1:n.17289A>G
NR_003149.2:n.17292A>G
ENST00000405460.6:c.17276A>G	ENSP00000384582.2:p.Asn5759Ser
ENST00000425867.2:c.4259A>G	ENSP00000392618.2:p.Asn1420Ser
ENST00000425867.3:c.6230A>G	ENSP00000392618.3:p.Asn2077Ser
ENST00000505845.2:n.467A>G
ENST00000638510.1:n.4543A>G
ENST00000638990.1:c.488A>G
ENST00000639431.1:c.266-131989A>G	ENSP00000491057.1:n.266-131989A>G
ENST00000640407.1:c.3725A>G	ENSP00000491425.1:n.3725A>G
XM_011543675.1:c.17273A>G	XP_011541977.1:p.Asn5758Ser
XM_011543676.1:c.17195A>G	XP_011541978.1:p.Asn5732Ser
XM_011543677.1:c.14579A>G	XP_011541979.1:p.Asn4860Ser
XM_017009963.2:c.17297A>G	XP_016865452.1:p.Asn5766Ser
XM_017009964.2:c.17294A>G	XP_016865453.1:p.Asn5765Ser
XM_017009965.1:c.17294A>G	XP_016865454.1:p.Asn5765Ser
XM_017009966.2:c.17216A>G	XP_016865455.1:p.Asn5739Ser
XM_017009967.1:c.17201A>G	XP_016865456.1:p.Asn5734Ser
XM_017009968.2:c.17117A>G	XP_016865457.1:p.Asn5706Ser
XM_017009969.2:c.17297A>G	XP_016865458.1:p.Asn5766Ser
XM_017009972.1:c.10415A>G	XP_016865461.1:p.Asn3472Ser
XM_017009973.1:c.10394A>G	XP_016865462.1:p.Asn3465Ser