Canonical Allele Identifier: CA360396249

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712347-G-T
• MyVariant Identifiers: chr5:g.90008164G>T (hg19) ; chr5:g.90712347G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712347G>T , CM000667.2:g.90712347G>T	GRCh38
NC_000005.9:g.90008164G>T , CM000667.1:g.90008164G>T	GRCh37
NC_000005.8:g.90043920G>T	NCBI36
NG_007083.1:g.158548G>T
NG_007083.2:g.188004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9103G>T MANE Select	ENSP00000384582.2:p.Asp3035Tyr
ENST00000639431.1:c.265+36138G>T	ENSP00000491057.1:n.265+36138G>T
ENST00000639473.1:n.4562G>T
ENST00000640012.1:c.2910G>T
ENST00000640374.1:n.2247G>T
ENST00000640779.1:c.3832G>T
ENST00000405460.6:c.9103G>T	ENSP00000384582.2:p.Asp3035Tyr
ENST00000509621.1:c.1800G>T
NM_032119.3:c.9103G>T	NP_115495.3:p.Asp3035Tyr
NR_003149.1:n.9116G>T
XM_011543675.1:c.9100G>T	XP_011541977.1:p.Asp3034Tyr
XM_011543676.1:c.9022G>T	XP_011541978.1:p.Asp3008Tyr
XM_011543677.1:c.6406G>T	XP_011541979.1:p.Asp2136Tyr
XM_011543678.1:c.9103G>T	XP_011541980.1:p.Asp3035Tyr
XM_011543679.1:c.9103G>T	XP_011541981.1:p.Asp3035Tyr
NM_032119.4:c.9103G>T MANE Select	NP_115495.3:p.Asp3035Tyr
XM_017009963.2:c.9124G>T	XP_016865452.1:p.Asp3042Tyr
XM_017009964.2:c.9121G>T	XP_016865453.1:p.Asp3041Tyr
XM_017009965.1:c.9121G>T	XP_016865454.1:p.Asp3041Tyr
XM_017009966.2:c.9043G>T	XP_016865455.1:p.Asp3015Tyr
XM_017009967.1:c.9028G>T	XP_016865456.1:p.Asp3010Tyr
XM_017009968.2:c.9124G>T	XP_016865457.1:p.Asp3042Tyr
XM_017009969.2:c.9124G>T	XP_016865458.1:p.Asp3042Tyr
XM_017009970.2:c.9124G>T	XP_016865459.1:p.Asp3042Tyr
XM_017009971.2:c.9124G>T	XP_016865460.1:p.Asp3042Tyr
XM_017009972.1:c.2242G>T	XP_016865461.1:p.Asp748Tyr
XM_017009973.1:c.2221G>T	XP_016865462.1:p.Asp741Tyr
XM_017009974.2:c.9124G>T	XP_016865463.1:p.Asp3042Tyr
NR_003149.2:n.9119G>T