Canonical Allele Identifier: CA3342348

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90853428A>G , CM000667.2:g.90853428A>G	GRCh38
NC_000005.9:g.90149245A>G , CM000667.1:g.90149245A>G	GRCh37
NC_000005.8:g.90185001A>G	NCBI36
NG_007083.1:g.299629A>G
NG_007083.2:g.329085A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17349A>G MANE Select	NP_115495.3:p.Ala5783=
ENST00000405460.9:c.17349A>G MANE Select	ENSP00000384582.2:p.Ala5783=
NM_032119.3:c.17349A>G	NP_115495.3:p.Ala5783=
NR_003149.1:n.17362A>G
NR_003149.2:n.17365A>G
ENST00000405460.6:c.17349A>G	ENSP00000384582.2:p.Ala5783=
ENST00000425867.2:c.4332A>G	ENSP00000392618.2:p.Ala1444=
ENST00000425867.3:c.6303A>G	ENSP00000392618.3:p.Ala2101=
ENST00000505845.2:n.540A>G
ENST00000638510.1:n.4616A>G
ENST00000638990.1:c.561A>G
ENST00000639431.1:c.266-131916A>G	ENSP00000491057.1:n.266-131916A>G
ENST00000640407.1:c.3798A>G	ENSP00000491425.1:n.3798A>G
XM_011543675.1:c.17346A>G	XP_011541977.1:p.Ala5782=
XM_011543676.1:c.17268A>G	XP_011541978.1:p.Ala5756=
XM_011543677.1:c.14652A>G	XP_011541979.1:p.Ala4884=
XM_017009963.2:c.17370A>G	XP_016865452.1:p.Ala5790=
XM_017009964.2:c.17367A>G	XP_016865453.1:p.Ala5789=
XM_017009965.1:c.17367A>G	XP_016865454.1:p.Ala5789=
XM_017009966.2:c.17289A>G	XP_016865455.1:p.Ala5763=
XM_017009967.1:c.17274A>G	XP_016865456.1:p.Ala5758=
XM_017009968.2:c.17190A>G	XP_016865457.1:p.Ala5730=
XM_017009969.2:c.17370A>G	XP_016865458.1:p.Ala5790=
XM_017009972.1:c.10488A>G	XP_016865461.1:p.Ala3496=
XM_017009973.1:c.10467A>G	XP_016865462.1:p.Ala3489=