Canonical Allele Identifier: CA360388725

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90703682-C-T
• MyVariant Identifiers: chr5:g.89999499C>T (hg19) ; chr5:g.90703682C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703682C>T , CM000667.2:g.90703682C>T	GRCh38
NC_000005.9:g.89999499C>T , CM000667.1:g.89999499C>T	GRCh37
NC_000005.8:g.90035255C>T	NCBI36
NG_007083.1:g.149883C>T
NG_007083.2:g.179339C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8173C>T MANE Select	ENSP00000384582.2:p.His2725Tyr
ENST00000639431.1:c.265+27473C>T	ENSP00000491057.1:n.265+27473C>T
ENST00000639473.1:n.3632C>T
ENST00000640012.1:c.1980C>T
ENST00000640374.1:n.1317C>T
ENST00000640403.1:c.5464C>T	ENSP00000492531.1:p.His1822Tyr
ENST00000640779.1:c.2902C>T
ENST00000405460.6:c.8173C>T	ENSP00000384582.2:p.His2725Tyr
ENST00000509621.1:c.870C>T
NM_032119.3:c.8173C>T	NP_115495.3:p.His2725Tyr
NR_003149.1:n.8186C>T
XM_011543675.1:c.8170C>T	XP_011541977.1:p.His2724Tyr
XM_011543676.1:c.8092C>T	XP_011541978.1:p.His2698Tyr
XM_011543677.1:c.5476C>T	XP_011541979.1:p.His1826Tyr
XM_011543678.1:c.8173C>T	XP_011541980.1:p.His2725Tyr
XM_011543679.1:c.8173C>T	XP_011541981.1:p.His2725Tyr
NM_032119.4:c.8173C>T MANE Select	NP_115495.3:p.His2725Tyr
XM_017009963.2:c.8173C>T	XP_016865452.1:p.His2725Tyr
XM_017009964.2:c.8170C>T	XP_016865453.1:p.His2724Tyr
XM_017009965.1:c.8170C>T	XP_016865454.1:p.His2724Tyr
XM_017009966.2:c.8092C>T	XP_016865455.1:p.His2698Tyr
XM_017009967.1:c.8077C>T	XP_016865456.1:p.His2693Tyr
XM_017009968.2:c.8173C>T	XP_016865457.1:p.His2725Tyr
XM_017009969.2:c.8173C>T	XP_016865458.1:p.His2725Tyr
XM_017009970.2:c.8173C>T	XP_016865459.1:p.His2725Tyr
XM_017009971.2:c.8173C>T	XP_016865460.1:p.His2725Tyr
XM_017009972.1:c.1291C>T	XP_016865461.1:p.His431Tyr
XM_017009973.1:c.1291C>T	XP_016865462.1:p.His431Tyr
XM_017009974.2:c.8173C>T	XP_016865463.1:p.His2725Tyr
NR_003149.2:n.8189C>T