Canonical Allele Identifier: CA360396131

Gene: ADGRV1

Linked Data

• dbSNP Id: rs769373495
• MyVariant Identifiers: chr5:g.90008113T>A (hg19) ; chr5:g.90712296T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712296T>A , CM000667.2:g.90712296T>A	GRCh38
NC_000005.9:g.90008113T>A , CM000667.1:g.90008113T>A	GRCh37
NC_000005.8:g.90043869T>A	NCBI36
NG_007083.1:g.158497T>A
NG_007083.2:g.187953T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9052T>A MANE Select	ENSP00000384582.2:p.Phe3018Ile
ENST00000639431.1:c.265+36087T>A	ENSP00000491057.1:n.265+36087T>A
ENST00000639473.1:n.4511T>A
ENST00000640012.1:c.2859T>A
ENST00000640374.1:n.2196T>A
ENST00000640779.1:c.3781T>A
ENST00000405460.6:c.9052T>A	ENSP00000384582.2:p.Phe3018Ile
ENST00000509621.1:c.1749T>A
NM_032119.3:c.9052T>A	NP_115495.3:p.Phe3018Ile
NR_003149.1:n.9065T>A
XM_011543675.1:c.9049T>A	XP_011541977.1:p.Phe3017Ile
XM_011543676.1:c.8971T>A	XP_011541978.1:p.Phe2991Ile
XM_011543677.1:c.6355T>A	XP_011541979.1:p.Phe2119Ile
XM_011543678.1:c.9052T>A	XP_011541980.1:p.Phe3018Ile
XM_011543679.1:c.9052T>A	XP_011541981.1:p.Phe3018Ile
NM_032119.4:c.9052T>A MANE Select	NP_115495.3:p.Phe3018Ile
XM_017009963.2:c.9073T>A	XP_016865452.1:p.Phe3025Ile
XM_017009964.2:c.9070T>A	XP_016865453.1:p.Phe3024Ile
XM_017009965.1:c.9070T>A	XP_016865454.1:p.Phe3024Ile
XM_017009966.2:c.8992T>A	XP_016865455.1:p.Phe2998Ile
XM_017009967.1:c.8977T>A	XP_016865456.1:p.Phe2993Ile
XM_017009968.2:c.9073T>A	XP_016865457.1:p.Phe3025Ile
XM_017009969.2:c.9073T>A	XP_016865458.1:p.Phe3025Ile
XM_017009970.2:c.9073T>A	XP_016865459.1:p.Phe3025Ile
XM_017009971.2:c.9073T>A	XP_016865460.1:p.Phe3025Ile
XM_017009972.1:c.2191T>A	XP_016865461.1:p.Phe731Ile
XM_017009973.1:c.2170T>A	XP_016865462.1:p.Phe724Ile
XM_017009974.2:c.9073T>A	XP_016865463.1:p.Phe3025Ile
NR_003149.2:n.9068T>A