Canonical Allele Identifier: CA3339683

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683813T>C , CM000667.2:g.90683813T>C	GRCh38
NC_000005.9:g.89979630T>C , CM000667.1:g.89979630T>C	GRCh37
NC_000005.8:g.90015386T>C	NCBI36
NG_007083.1:g.130014T>C
NG_007083.2:g.159470T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5892T>C MANE Select	NP_115495.3:p.Asn1964=
ENST00000405460.9:c.5892T>C MANE Select	ENSP00000384582.2:p.Asn1964=
NM_032119.3:c.5892T>C	NP_115495.3:p.Asn1964=
NR_003149.1:n.5988T>C
NR_003149.2:n.5991T>C
ENST00000405460.6:c.5892T>C	ENSP00000384582.2:p.Asn1964=
ENST00000639431.1:c.265+7604T>C	ENSP00000491057.1:n.265+7604T>C
ENST00000639473.1:n.1351T>C
ENST00000640012.1:c.165-1967T>C
ENST00000640403.1:c.3183T>C	ENSP00000492531.1:p.Asn1061=
ENST00000640779.1:c.704T>C
XM_011543675.1:c.5889T>C	XP_011541977.1:p.Asn1963=
XM_011543676.1:c.5811T>C	XP_011541978.1:p.Asn1937=
XM_011543677.1:c.3195T>C	XP_011541979.1:p.Asn1065=
XM_011543678.1:c.5892T>C	XP_011541980.1:p.Asn1964=
XM_011543679.1:c.5892T>C	XP_011541981.1:p.Asn1964=
XM_017009963.2:c.5892T>C	XP_016865452.1:p.Asn1964=
XM_017009964.2:c.5889T>C	XP_016865453.1:p.Asn1963=
XM_017009965.1:c.5889T>C	XP_016865454.1:p.Asn1963=
XM_017009966.2:c.5811T>C	XP_016865455.1:p.Asn1937=
XM_017009967.1:c.5796T>C	XP_016865456.1:p.Asn1932=
XM_017009968.2:c.5892T>C	XP_016865457.1:p.Asn1964=
XM_017009969.2:c.5892T>C	XP_016865458.1:p.Asn1964=
XM_017009970.2:c.5892T>C	XP_016865459.1:p.Asn1964=
XM_017009971.2:c.5892T>C	XP_016865460.1:p.Asn1964=
XM_017009973.1:c.-908T>C	XP_016865462.1:n.-908T>C
XM_017009974.2:c.5892T>C	XP_016865463.1:p.Asn1964=