Canonical Allele Identifier: CA3339699

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 935715
• ClinVar RCV Id: RCV001204363
• dbSNP Id: rs766508393
• ExAC: 5:89979782 A / T
• gnomAD v2: 5-89979782-A-T
• gnomAD v3: 5-90683965-A-T
• gnomAD v4: 5-90683965-A-T
• MyVariant Identifiers: chr5:g.89979782A>T (hg19) ; chr5:g.90683965A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683965A>T , CM000667.2:g.90683965A>T	GRCh38
NC_000005.9:g.89979782A>T , CM000667.1:g.89979782A>T	GRCh37
NC_000005.8:g.90015538A>T	NCBI36
NG_007083.1:g.130166A>T
NG_007083.2:g.159622A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6044A>T MANE Select	ENSP00000384582.2:p.Tyr2015Phe
ENST00000639431.1:c.265+7756A>T	ENSP00000491057.1:n.265+7756A>T
ENST00000639473.1:n.1503A>T
ENST00000640012.1:c.165-1815A>T
ENST00000640403.1:c.3335A>T	ENSP00000492531.1:p.Tyr1112Phe
ENST00000640779.1:c.856A>T
ENST00000405460.6:c.6044A>T	ENSP00000384582.2:p.Tyr2015Phe
NM_032119.3:c.6044A>T	NP_115495.3:p.Tyr2015Phe
NR_003149.1:n.6140A>T
XM_011543675.1:c.6041A>T	XP_011541977.1:p.Tyr2014Phe
XM_011543676.1:c.5963A>T	XP_011541978.1:p.Tyr1988Phe
XM_011543677.1:c.3347A>T	XP_011541979.1:p.Tyr1116Phe
XM_011543678.1:c.6044A>T	XP_011541980.1:p.Tyr2015Phe
XM_011543679.1:c.6044A>T	XP_011541981.1:p.Tyr2015Phe
NM_032119.4:c.6044A>T MANE Select	NP_115495.3:p.Tyr2015Phe
XM_017009963.2:c.6044A>T	XP_016865452.1:p.Tyr2015Phe
XM_017009964.2:c.6041A>T	XP_016865453.1:p.Tyr2014Phe
XM_017009965.1:c.6041A>T	XP_016865454.1:p.Tyr2014Phe
XM_017009966.2:c.5963A>T	XP_016865455.1:p.Tyr1988Phe
XM_017009967.1:c.5948A>T	XP_016865456.1:p.Tyr1983Phe
XM_017009968.2:c.6044A>T	XP_016865457.1:p.Tyr2015Phe
XM_017009969.2:c.6044A>T	XP_016865458.1:p.Tyr2015Phe
XM_017009970.2:c.6044A>T	XP_016865459.1:p.Tyr2015Phe
XM_017009971.2:c.6044A>T	XP_016865460.1:p.Tyr2015Phe
XM_017009973.1:c.-756A>T	XP_016865462.1:n.-756A>T
XM_017009974.2:c.6044A>T	XP_016865463.1:p.Tyr2015Phe
NR_003149.2:n.6143A>T