Canonical Allele Identifier: CA360396133

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008114T>A (hg19) ; chr5:g.90712297T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712297T>A , CM000667.2:g.90712297T>A	GRCh38
NC_000005.9:g.90008114T>A , CM000667.1:g.90008114T>A	GRCh37
NC_000005.8:g.90043870T>A	NCBI36
NG_007083.1:g.158498T>A
NG_007083.2:g.187954T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9053T>A MANE Select	ENSP00000384582.2:p.Phe3018Tyr
ENST00000639431.1:c.265+36088T>A	ENSP00000491057.1:n.265+36088T>A
ENST00000639473.1:n.4512T>A
ENST00000640012.1:c.2860T>A
ENST00000640374.1:n.2197T>A
ENST00000640779.1:c.3782T>A
ENST00000405460.6:c.9053T>A	ENSP00000384582.2:p.Phe3018Tyr
ENST00000509621.1:c.1750T>A
NM_032119.3:c.9053T>A	NP_115495.3:p.Phe3018Tyr
NR_003149.1:n.9066T>A
XM_011543675.1:c.9050T>A	XP_011541977.1:p.Phe3017Tyr
XM_011543676.1:c.8972T>A	XP_011541978.1:p.Phe2991Tyr
XM_011543677.1:c.6356T>A	XP_011541979.1:p.Phe2119Tyr
XM_011543678.1:c.9053T>A	XP_011541980.1:p.Phe3018Tyr
XM_011543679.1:c.9053T>A	XP_011541981.1:p.Phe3018Tyr
NM_032119.4:c.9053T>A MANE Select	NP_115495.3:p.Phe3018Tyr
XM_017009963.2:c.9074T>A	XP_016865452.1:p.Phe3025Tyr
XM_017009964.2:c.9071T>A	XP_016865453.1:p.Phe3024Tyr
XM_017009965.1:c.9071T>A	XP_016865454.1:p.Phe3024Tyr
XM_017009966.2:c.8993T>A	XP_016865455.1:p.Phe2998Tyr
XM_017009967.1:c.8978T>A	XP_016865456.1:p.Phe2993Tyr
XM_017009968.2:c.9074T>A	XP_016865457.1:p.Phe3025Tyr
XM_017009969.2:c.9074T>A	XP_016865458.1:p.Phe3025Tyr
XM_017009970.2:c.9074T>A	XP_016865459.1:p.Phe3025Tyr
XM_017009971.2:c.9074T>A	XP_016865460.1:p.Phe3025Tyr
XM_017009972.1:c.2192T>A	XP_016865461.1:p.Phe731Tyr
XM_017009973.1:c.2171T>A	XP_016865462.1:p.Phe724Tyr
XM_017009974.2:c.9074T>A	XP_016865463.1:p.Phe3025Tyr
NR_003149.2:n.9069T>A