Canonical Allele Identifier: CA3341457

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90781533G>A , CM000667.2:g.90781533G>A	GRCh38
NC_000005.9:g.90077350G>A , CM000667.1:g.90077350G>A	GRCh37
NC_000005.8:g.90113106G>A	NCBI36
NG_007083.1:g.227734G>A
NG_007083.2:g.257190G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13186G>A MANE Select	NP_115495.3:p.Ala4396Thr
ENST00000405460.9:c.13186G>A MANE Select	ENSP00000384582.2:p.Ala4396Thr
NM_032119.3:c.13186G>A	NP_115495.3:p.Ala4396Thr
NR_003149.1:n.13199G>A
NR_003149.2:n.13202G>A
ENST00000405460.6:c.13186G>A	ENSP00000384582.2:p.Ala4396Thr
ENST00000425867.2:c.169G>A	ENSP00000392618.2:p.Ala57Thr
ENST00000425867.3:c.2140G>A	ENSP00000392618.3:p.Ala714Thr
ENST00000638510.1:n.453G>A
ENST00000639431.1:c.265+105324G>A	ENSP00000491057.1:n.265+105324G>A
XM_011543675.1:c.13183G>A	XP_011541977.1:p.Ala4395Thr
XM_011543676.1:c.13105G>A	XP_011541978.1:p.Ala4369Thr
XM_011543677.1:c.10489G>A	XP_011541979.1:p.Ala3497Thr
XM_011543678.1:c.13186G>A	XP_011541980.1:p.Ala4396Thr
XM_017009963.2:c.13207G>A	XP_016865452.1:p.Ala4403Thr
XM_017009964.2:c.13204G>A	XP_016865453.1:p.Ala4402Thr
XM_017009965.1:c.13204G>A	XP_016865454.1:p.Ala4402Thr
XM_017009966.2:c.13126G>A	XP_016865455.1:p.Ala4376Thr
XM_017009967.1:c.13111G>A	XP_016865456.1:p.Ala4371Thr
XM_017009968.2:c.13207G>A	XP_016865457.1:p.Ala4403Thr
XM_017009969.2:c.13207G>A	XP_016865458.1:p.Ala4403Thr
XM_017009970.2:c.13207G>A	XP_016865459.1:p.Ala4403Thr
XM_017009971.2:c.13207G>A	XP_016865460.1:p.Ala4403Thr
XM_017009972.1:c.6325G>A	XP_016865461.1:p.Ala2109Thr
XM_017009973.1:c.6304G>A	XP_016865462.1:p.Ala2102Thr