Canonical Allele Identifier: CA360396326

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008198T>A (hg19) ; chr5:g.90712381T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712381T>A , CM000667.2:g.90712381T>A	GRCh38
NC_000005.9:g.90008198T>A , CM000667.1:g.90008198T>A	GRCh37
NC_000005.8:g.90043954T>A	NCBI36
NG_007083.1:g.158582T>A
NG_007083.2:g.188038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9137T>A MANE Select	ENSP00000384582.2:p.Ile3046Asn
ENST00000639431.1:c.265+36172T>A	ENSP00000491057.1:n.265+36172T>A
ENST00000639473.1:n.4596T>A
ENST00000640012.1:c.2944T>A
ENST00000640374.1:n.2281T>A
ENST00000640779.1:c.3866T>A
ENST00000405460.6:c.9137T>A	ENSP00000384582.2:p.Ile3046Asn
ENST00000509621.1:c.1834T>A
NM_032119.3:c.9137T>A	NP_115495.3:p.Ile3046Asn
NR_003149.1:n.9150T>A
XM_011543675.1:c.9134T>A	XP_011541977.1:p.Ile3045Asn
XM_011543676.1:c.9056T>A	XP_011541978.1:p.Ile3019Asn
XM_011543677.1:c.6440T>A	XP_011541979.1:p.Ile2147Asn
XM_011543678.1:c.9137T>A	XP_011541980.1:p.Ile3046Asn
XM_011543679.1:c.9137T>A	XP_011541981.1:p.Ile3046Asn
XR_948560.1:n.465A>T
NM_032119.4:c.9137T>A MANE Select	NP_115495.3:p.Ile3046Asn
XM_017009963.2:c.9158T>A	XP_016865452.1:p.Ile3053Asn
XM_017009964.2:c.9155T>A	XP_016865453.1:p.Ile3052Asn
XM_017009965.1:c.9155T>A	XP_016865454.1:p.Ile3052Asn
XM_017009966.2:c.9077T>A	XP_016865455.1:p.Ile3026Asn
XM_017009967.1:c.9062T>A	XP_016865456.1:p.Ile3021Asn
XM_017009968.2:c.9158T>A	XP_016865457.1:p.Ile3053Asn
XM_017009969.2:c.9158T>A	XP_016865458.1:p.Ile3053Asn
XM_017009970.2:c.9158T>A	XP_016865459.1:p.Ile3053Asn
XM_017009971.2:c.9158T>A	XP_016865460.1:p.Ile3053Asn
XM_017009972.1:c.2276T>A	XP_016865461.1:p.Ile759Asn
XM_017009973.1:c.2255T>A	XP_016865462.1:p.Ile752Asn
XM_017009974.2:c.9158T>A	XP_016865463.1:p.Ile3053Asn
NR_003149.2:n.9153T>A