Canonical Allele Identifier: CA445406319

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90763307-A-G
• MyVariant Identifiers: chr5:g.90059124A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763307A>G , CM000667.2:g.90763307A>G	GRCh38
NC_000005.9:g.90059124A>G , CM000667.1:g.90059124A>G	GRCh37
NC_000005.8:g.90094880A>G	NCBI36
NG_007083.1:g.209508A>G
NG_007083.2:g.238964A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12123A>G MANE Select	ENSP00000384582.2:p.Val4041=
ENST00000425867.3:c.1077A>G	ENSP00000392618.3:p.Val359=
ENST00000639431.1:c.265+87098A>G	ENSP00000491057.1:n.265+87098A>G
ENST00000640464.1:n.2542A>G
ENST00000640729.1:n.700A>G
ENST00000405460.6:c.12123A>G	ENSP00000384582.2:p.Val4041=
NM_032119.3:c.12123A>G	NP_115495.3:p.Val4041=
NR_003149.1:n.12136A>G
XM_011543675.1:c.12120A>G	XP_011541977.1:p.Val4040=
XM_011543676.1:c.12042A>G	XP_011541978.1:p.Val4014=
XM_011543677.1:c.9426A>G	XP_011541979.1:p.Val3142=
XM_011543678.1:c.12123A>G	XP_011541980.1:p.Val4041=
NM_032119.4:c.12123A>G MANE Select	NP_115495.3:p.Val4041=
XM_017009963.2:c.12144A>G	XP_016865452.1:p.Val4048=
XM_017009964.2:c.12141A>G	XP_016865453.1:p.Val4047=
XM_017009965.1:c.12141A>G	XP_016865454.1:p.Val4047=
XM_017009966.2:c.12063A>G	XP_016865455.1:p.Val4021=
XM_017009967.1:c.12048A>G	XP_016865456.1:p.Val4016=
XM_017009968.2:c.12144A>G	XP_016865457.1:p.Val4048=
XM_017009969.2:c.12144A>G	XP_016865458.1:p.Val4048=
XM_017009970.2:c.12144A>G	XP_016865459.1:p.Val4048=
XM_017009971.2:c.12144A>G	XP_016865460.1:p.Val4048=
XM_017009972.1:c.5262A>G	XP_016865461.1:p.Val1754=
XM_017009973.1:c.5241A>G	XP_016865462.1:p.Val1747=
NR_003149.2:n.12139A>G