Canonical Allele Identifier: CA360396144

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712302-G-T
• MyVariant Identifiers: chr5:g.90008119G>T (hg19) ; chr5:g.90712302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712302G>T , CM000667.2:g.90712302G>T	GRCh38
NC_000005.9:g.90008119G>T , CM000667.1:g.90008119G>T	GRCh37
NC_000005.8:g.90043875G>T	NCBI36
NG_007083.1:g.158503G>T
NG_007083.2:g.187959G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9058G>T MANE Select	ENSP00000384582.2:p.Asp3020Tyr
ENST00000639431.1:c.265+36093G>T	ENSP00000491057.1:n.265+36093G>T
ENST00000639473.1:n.4517G>T
ENST00000640012.1:c.2865G>T
ENST00000640374.1:n.2202G>T
ENST00000640779.1:c.3787G>T
ENST00000405460.6:c.9058G>T	ENSP00000384582.2:p.Asp3020Tyr
ENST00000509621.1:c.1755G>T
NM_032119.3:c.9058G>T	NP_115495.3:p.Asp3020Tyr
NR_003149.1:n.9071G>T
XM_011543675.1:c.9055G>T	XP_011541977.1:p.Asp3019Tyr
XM_011543676.1:c.8977G>T	XP_011541978.1:p.Asp2993Tyr
XM_011543677.1:c.6361G>T	XP_011541979.1:p.Asp2121Tyr
XM_011543678.1:c.9058G>T	XP_011541980.1:p.Asp3020Tyr
XM_011543679.1:c.9058G>T	XP_011541981.1:p.Asp3020Tyr
NM_032119.4:c.9058G>T MANE Select	NP_115495.3:p.Asp3020Tyr
XM_017009963.2:c.9079G>T	XP_016865452.1:p.Asp3027Tyr
XM_017009964.2:c.9076G>T	XP_016865453.1:p.Asp3026Tyr
XM_017009965.1:c.9076G>T	XP_016865454.1:p.Asp3026Tyr
XM_017009966.2:c.8998G>T	XP_016865455.1:p.Asp3000Tyr
XM_017009967.1:c.8983G>T	XP_016865456.1:p.Asp2995Tyr
XM_017009968.2:c.9079G>T	XP_016865457.1:p.Asp3027Tyr
XM_017009969.2:c.9079G>T	XP_016865458.1:p.Asp3027Tyr
XM_017009970.2:c.9079G>T	XP_016865459.1:p.Asp3027Tyr
XM_017009971.2:c.9079G>T	XP_016865460.1:p.Asp3027Tyr
XM_017009972.1:c.2197G>T	XP_016865461.1:p.Asp733Tyr
XM_017009973.1:c.2176G>T	XP_016865462.1:p.Asp726Tyr
XM_017009974.2:c.9079G>T	XP_016865463.1:p.Asp3027Tyr
NR_003149.2:n.9074G>T