Canonical Allele Identifier: CA3342281

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90848650G>C , CM000667.2:g.90848650G>C	GRCh38
NC_000005.9:g.90144467G>C , CM000667.1:g.90144467G>C	GRCh37
NC_000005.8:g.90180223G>C	NCBI36
NG_007083.1:g.294851G>C
NG_007083.2:g.324307G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17033G>C MANE Select	NP_115495.3:p.Gly5678Ala
ENST00000405460.9:c.17033G>C MANE Select	ENSP00000384582.2:p.Gly5678Ala
NM_032119.3:c.17033G>C	NP_115495.3:p.Gly5678Ala
NR_003149.1:n.17046G>C
NR_003149.2:n.17049G>C
ENST00000405460.6:c.17033G>C	ENSP00000384582.2:p.Gly5678Ala
ENST00000425867.2:c.4016G>C	ENSP00000392618.2:p.Gly1339Ala
ENST00000425867.3:c.5987G>C	ENSP00000392618.3:p.Gly1996Ala
ENST00000505845.1:n.224G>C
ENST00000505845.2:n.224G>C
ENST00000638510.1:n.4300G>C
ENST00000638990.1:c.54G>C
ENST00000639431.1:c.266-136694G>C	ENSP00000491057.1:n.266-136694G>C
ENST00000640061.1:n.550G>C
ENST00000640407.1:c.3482G>C	ENSP00000491425.1:n.3482G>C
XM_011543675.1:c.17030G>C	XP_011541977.1:p.Gly5677Ala
XM_011543676.1:c.16952G>C	XP_011541978.1:p.Gly5651Ala
XM_011543677.1:c.14336G>C	XP_011541979.1:p.Gly4779Ala
XM_017009963.2:c.17054G>C	XP_016865452.1:p.Gly5685Ala
XM_017009964.2:c.17051G>C	XP_016865453.1:p.Gly5684Ala
XM_017009965.1:c.17051G>C	XP_016865454.1:p.Gly5684Ala
XM_017009966.2:c.16973G>C	XP_016865455.1:p.Gly5658Ala
XM_017009967.1:c.16958G>C	XP_016865456.1:p.Gly5653Ala
XM_017009968.2:c.16874G>C	XP_016865457.1:p.Gly5625Ala
XM_017009969.2:c.17054G>C	XP_016865458.1:p.Gly5685Ala
XM_017009972.1:c.10172G>C	XP_016865461.1:p.Gly3391Ala
XM_017009973.1:c.10151G>C	XP_016865462.1:p.Gly3384Ala