Canonical Allele Identifier: CA360367187

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050965A>G (hg19) ; chr5:g.90755148A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755148A>G , CM000667.2:g.90755148A>G	GRCh38
NC_000005.9:g.90050965A>G , CM000667.1:g.90050965A>G	GRCh37
NC_000005.8:g.90086721A>G	NCBI36
NG_007083.1:g.201349A>G
NG_007083.2:g.230805A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11543A>G MANE Select	ENSP00000384582.2:p.Asn3848Ser
ENST00000425867.3:c.674A>G	ENSP00000392618.3:p.Asn225Ser
ENST00000639431.1:c.265+78939A>G	ENSP00000491057.1:n.265+78939A>G
ENST00000640374.1:n.4687A>G
ENST00000640464.1:n.1962A>G
ENST00000405460.6:c.11543A>G	ENSP00000384582.2:p.Asn3848Ser
ENST00000509621.1:c.4240A>G
NM_032119.3:c.11543A>G	NP_115495.3:p.Asn3848Ser
NR_003149.1:n.11556A>G
XM_011543675.1:c.11540A>G	XP_011541977.1:p.Asn3847Ser
XM_011543676.1:c.11462A>G	XP_011541978.1:p.Asn3821Ser
XM_011543677.1:c.8846A>G	XP_011541979.1:p.Asn2949Ser
XM_011543678.1:c.11543A>G	XP_011541980.1:p.Asn3848Ser
NM_032119.4:c.11543A>G MANE Select	NP_115495.3:p.Asn3848Ser
XM_017009963.2:c.11564A>G	XP_016865452.1:p.Asn3855Ser
XM_017009964.2:c.11561A>G	XP_016865453.1:p.Asn3854Ser
XM_017009965.1:c.11561A>G	XP_016865454.1:p.Asn3854Ser
XM_017009966.2:c.11483A>G	XP_016865455.1:p.Asn3828Ser
XM_017009967.1:c.11468A>G	XP_016865456.1:p.Asn3823Ser
XM_017009968.2:c.11564A>G	XP_016865457.1:p.Asn3855Ser
XM_017009969.2:c.11564A>G	XP_016865458.1:p.Asn3855Ser
XM_017009970.2:c.11564A>G	XP_016865459.1:p.Asn3855Ser
XM_017009971.2:c.11564A>G	XP_016865460.1:p.Asn3855Ser
XM_017009972.1:c.4682A>G	XP_016865461.1:p.Asn1561Ser
XM_017009973.1:c.4661A>G	XP_016865462.1:p.Asn1554Ser
NR_003149.2:n.11559A>G