Canonical Allele Identifier: CA360362801

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90750608G>A , CM000667.2:g.90750608G>A	GRCh38
NC_000005.9:g.90046425G>A , CM000667.1:g.90046425G>A	GRCh37
NC_000005.8:g.90082181G>A	NCBI36
NG_007083.1:g.196809G>A
NG_007083.2:g.226265G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11032G>A MANE Select	NP_115495.3:p.Val3678Ile
ENST00000405460.9:c.11032G>A MANE Select	ENSP00000384582.2:p.Val3678Ile
NM_032119.3:c.11032G>A	NP_115495.3:p.Val3678Ile
NR_003149.1:n.11045G>A
NR_003149.2:n.11048G>A
ENST00000405460.6:c.11032G>A	ENSP00000384582.2:p.Val3678Ile
ENST00000425867.3:c.163G>A	ENSP00000392618.3:p.Val55Ile
ENST00000509621.1:c.3729G>A
ENST00000639431.1:c.265+74399G>A	ENSP00000491057.1:n.265+74399G>A
ENST00000640374.1:n.4176G>A
ENST00000640464.1:n.1451G>A
XM_011543675.1:c.11029G>A	XP_011541977.1:p.Val3677Ile
XM_011543676.1:c.10951G>A	XP_011541978.1:p.Val3651Ile
XM_011543677.1:c.8335G>A	XP_011541979.1:p.Val2779Ile
XM_011543678.1:c.11032G>A	XP_011541980.1:p.Val3678Ile
XM_017009963.2:c.11053G>A	XP_016865452.1:p.Val3685Ile
XM_017009964.2:c.11050G>A	XP_016865453.1:p.Val3684Ile
XM_017009965.1:c.11050G>A	XP_016865454.1:p.Val3684Ile
XM_017009966.2:c.10972G>A	XP_016865455.1:p.Val3658Ile
XM_017009967.1:c.10957G>A	XP_016865456.1:p.Val3653Ile
XM_017009968.2:c.11053G>A	XP_016865457.1:p.Val3685Ile
XM_017009969.2:c.11053G>A	XP_016865458.1:p.Val3685Ile
XM_017009970.2:c.11053G>A	XP_016865459.1:p.Val3685Ile
XM_017009971.2:c.11053G>A	XP_016865460.1:p.Val3685Ile
XM_017009972.1:c.4171G>A	XP_016865461.1:p.Val1391Ile
XM_017009973.1:c.4150G>A	XP_016865462.1:p.Val1384Ile