Canonical Allele Identifier: CA3342726

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91153307G>A , CM000667.2:g.91153307G>A	GRCh38
NC_000005.9:g.90449124G>A , CM000667.1:g.90449124G>A	GRCh37
NC_000005.8:g.90484880G>A	NCBI36
NG_007083.1:g.599508G>A
NG_007083.2:g.628964G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18711G>A MANE Select	NP_115495.3:p.Thr6237=
ENST00000405460.9:c.18711G>A MANE Select	ENSP00000384582.2:p.Thr6237=
NM_032119.3:c.18711G>A	NP_115495.3:p.Thr6237=
NR_003149.1:n.18724G>A
NR_003149.2:n.18727G>A
ENST00000405460.6:c.18711G>A	ENSP00000384582.2:p.Thr6237=
ENST00000425867.2:c.5694G>A	ENSP00000392618.2:p.Thr1898=
ENST00000425867.3:c.7665G>A	ENSP00000392618.3:p.Thr2555=
ENST00000638510.1:n.5978G>A
ENST00000638990.1:c.1923G>A
ENST00000639212.1:n.631G>A
ENST00000639530.1:n.579G>A
ENST00000639821.1:c.517-10475G>A	ENSP00000492216.1:n.517-10475G>A
ENST00000640256.1:n.387G>A
ENST00000640407.1:c.5160G>A	ENSP00000491425.1:n.5160G>A
ENST00000640815.1:c.795G>A	ENSP00000491767.1:p.Thr265=
XM_011543675.1:c.18708G>A	XP_011541977.1:p.Thr6236=
XM_011543676.1:c.18630G>A	XP_011541978.1:p.Thr6210=
XM_011543677.1:c.16014G>A	XP_011541979.1:p.Thr5338=
XM_017009963.2:c.18732G>A	XP_016865452.1:p.Thr6244=
XM_017009964.2:c.18729G>A	XP_016865453.1:p.Thr6243=
XM_017009965.1:c.18729G>A	XP_016865454.1:p.Thr6243=
XM_017009966.2:c.18651G>A	XP_016865455.1:p.Thr6217=
XM_017009967.1:c.18636G>A	XP_016865456.1:p.Thr6212=
XM_017009968.2:c.18552G>A	XP_016865457.1:p.Thr6184=
XM_017009969.2:c.18454-10475G>A	XP_016865458.1:n.18454-10475G>A
XM_017009972.1:c.11850G>A	XP_016865461.1:p.Thr3950=
XM_017009973.1:c.11829G>A	XP_016865462.1:p.Thr3943=
XR_001742795.1:n.225-1119C>T
XR_001742796.1:n.225-17313C>T