Canonical Allele Identifier: CA360399168

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90789846-A-G
• MyVariant Identifiers: chr5:g.90085663A>G (hg19) ; chr5:g.90789846A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789846A>G , CM000667.2:g.90789846A>G	GRCh38
NC_000005.9:g.90085663A>G , CM000667.1:g.90085663A>G	GRCh37
NC_000005.8:g.90121419A>G	NCBI36
NG_007083.1:g.236047A>G
NG_007083.2:g.265503A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14038A>G MANE Select	ENSP00000384582.2:p.Ile4680Val
ENST00000425867.3:c.2992A>G	ENSP00000392618.3:p.Ile998Val
ENST00000638510.1:n.1305A>G
ENST00000638975.1:c.667A>G	ENSP00000492630.1:p.Ile223Val
ENST00000639431.1:c.265+113637A>G	ENSP00000491057.1:n.265+113637A>G
ENST00000640407.1:c.448A>G	ENSP00000491425.1:p.Ile150Val
ENST00000405460.6:c.14038A>G	ENSP00000384582.2:p.Ile4680Val
ENST00000425867.2:c.1021A>G	ENSP00000392618.2:p.Ile341Val
NM_032119.3:c.14038A>G	NP_115495.3:p.Ile4680Val
NR_003149.1:n.14051A>G
XM_011543675.1:c.14035A>G	XP_011541977.1:p.Ile4679Val
XM_011543676.1:c.13957A>G	XP_011541978.1:p.Ile4653Val
XM_011543677.1:c.11341A>G	XP_011541979.1:p.Ile3781Val
XM_011543678.1:c.14038A>G	XP_011541980.1:p.Ile4680Val
NM_032119.4:c.14038A>G MANE Select	NP_115495.3:p.Ile4680Val
XM_017009963.2:c.14059A>G	XP_016865452.1:p.Ile4687Val
XM_017009964.2:c.14056A>G	XP_016865453.1:p.Ile4686Val
XM_017009965.1:c.14056A>G	XP_016865454.1:p.Ile4686Val
XM_017009966.2:c.13978A>G	XP_016865455.1:p.Ile4660Val
XM_017009967.1:c.13963A>G	XP_016865456.1:p.Ile4655Val
XM_017009968.2:c.14059A>G	XP_016865457.1:p.Ile4687Val
XM_017009969.2:c.14059A>G	XP_016865458.1:p.Ile4687Val
XM_017009970.2:c.14059A>G	XP_016865459.1:p.Ile4687Val
XM_017009971.2:c.14059A>G	XP_016865460.1:p.Ile4687Val
XM_017009972.1:c.7177A>G	XP_016865461.1:p.Ile2393Val
XM_017009973.1:c.7156A>G	XP_016865462.1:p.Ile2386Val
NR_003149.2:n.14054A>G