Canonical Allele Identifier: CA360429418

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985523G>T , CM000667.2:g.90985523G>T	GRCh38
NC_000005.9:g.90281340G>T , CM000667.1:g.90281340G>T	GRCh37
NC_000005.8:g.90317096G>T	NCBI36
NG_007083.1:g.431724G>T
NG_007083.2:g.461180G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18152+1G>T MANE Select	NP_115495.3:n.18152+1G>T
ENST00000405460.9:c.18152+1G>T MANE Select	ENSP00000384582.2:n.18152+1G>T
NM_032119.3:c.18152+1G>T	NP_115495.3:n.18152+1G>T
NR_003149.1:n.18165+1G>T
NR_003149.2:n.18168+1G>T
ENST00000405460.6:c.18152+1G>T	ENSP00000384582.2:n.18152+1G>T
ENST00000425867.2:c.5135+1G>T	ENSP00000392618.2:n.5135+1G>T
ENST00000425867.3:c.7106+1G>T	ENSP00000392618.3:n.7106+1G>T
ENST00000638510.1:n.5419+1G>T
ENST00000638990.1:c.1364+1G>T
ENST00000639431.1:c.444+1G>T	ENSP00000491057.1:n.444+1G>T
ENST00000639707.1:c.236+1G>T	ENSP00000492328.1:n.236+1G>T
ENST00000639821.1:c.236+1G>T	ENSP00000492216.1:n.236+1G>T
ENST00000640369.1:c.236+1G>T	ENSP00000491401.1:n.236+1G>T
ENST00000640407.1:c.4601+1G>T	ENSP00000491425.1:n.4601+1G>T
ENST00000640815.1:c.236+1G>T	ENSP00000491767.1:n.236+1G>T
XM_011543675.1:c.18149+1G>T	XP_011541977.1:n.18149+1G>T
XM_011543676.1:c.18071+1G>T	XP_011541978.1:n.18071+1G>T
XM_011543677.1:c.15455+1G>T	XP_011541979.1:n.15455+1G>T
XM_017009963.2:c.18173+1G>T	XP_016865452.1:n.18173+1G>T
XM_017009964.2:c.18170+1G>T	XP_016865453.1:n.18170+1G>T
XM_017009965.1:c.18170+1G>T	XP_016865454.1:n.18170+1G>T
XM_017009966.2:c.18092+1G>T	XP_016865455.1:n.18092+1G>T
XM_017009967.1:c.18077+1G>T	XP_016865456.1:n.18077+1G>T
XM_017009968.2:c.17993+1G>T	XP_016865457.1:n.17993+1G>T
XM_017009969.2:c.18173+1G>T	XP_016865458.1:n.18173+1G>T
XM_017009972.1:c.11291+1G>T	XP_016865461.1:n.11291+1G>T
XM_017009973.1:c.11270+1G>T	XP_016865462.1:n.11270+1G>T