Canonical Allele Identifier: CA138000

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90750607C>T , CM000667.2:g.90750607C>T	GRCh38
NC_000005.9:g.90046424C>T , CM000667.1:g.90046424C>T	GRCh37
NC_000005.8:g.90082180C>T	NCBI36
NG_007083.1:g.196808C>T
NG_007083.2:g.226264C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11031C>T MANE Select	ENSP00000384582.2:p.Asn3677=
ENST00000425867.3:c.162C>T	ENSP00000392618.3:p.Asn54=
ENST00000639431.1:c.265+74398C>T	ENSP00000491057.1:n.265+74398C>T
ENST00000640374.1:n.4175C>T
ENST00000640464.1:n.1450C>T
ENST00000405460.6:c.11031C>T	ENSP00000384582.2:p.Asn3677=
ENST00000509621.1:c.3728C>T
NM_032119.3:c.11031C>T	NP_115495.3:p.Asn3677=
NR_003149.1:n.11044C>T
XM_011543675.1:c.11028C>T	XP_011541977.1:p.Asn3676=
XM_011543676.1:c.10950C>T	XP_011541978.1:p.Asn3650=
XM_011543677.1:c.8334C>T	XP_011541979.1:p.Asn2778=
XM_011543678.1:c.11031C>T	XP_011541980.1:p.Asn3677=
NM_032119.4:c.11031C>T MANE Select	NP_115495.3:p.Asn3677=
XM_017009963.2:c.11052C>T	XP_016865452.1:p.Asn3684=
XM_017009964.2:c.11049C>T	XP_016865453.1:p.Asn3683=
XM_017009965.1:c.11049C>T	XP_016865454.1:p.Asn3683=
XM_017009966.2:c.10971C>T	XP_016865455.1:p.Asn3657=
XM_017009967.1:c.10956C>T	XP_016865456.1:p.Asn3652=
XM_017009968.2:c.11052C>T	XP_016865457.1:p.Asn3684=
XM_017009969.2:c.11052C>T	XP_016865458.1:p.Asn3684=
XM_017009970.2:c.11052C>T	XP_016865459.1:p.Asn3684=
XM_017009971.2:c.11052C>T	XP_016865460.1:p.Asn3684=
XM_017009972.1:c.4170C>T	XP_016865461.1:p.Asn1390=
XM_017009973.1:c.4149C>T	XP_016865462.1:p.Asn1383=
NR_003149.2:n.11047C>T