Canonical Allele Identifier: CA360372050

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 2271634
• ClinVar RCV Id: RCV002794670
• MyVariant Identifiers: chr5:g.89988589A>G (hg19) ; chr5:g.90692772A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692772A>G , CM000667.2:g.90692772A>G	GRCh38
NC_000005.9:g.89988589A>G , CM000667.1:g.89988589A>G	GRCh37
NC_000005.8:g.90024345A>G	NCBI36
NG_007083.1:g.138973A>G
NG_007083.2:g.168429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7119A>G MANE Select	ENSP00000384582.2:p.Ile2373Met
ENST00000639431.1:c.265+16563A>G	ENSP00000491057.1:n.265+16563A>G
ENST00000639473.1:n.2578A>G
ENST00000640012.1:c.926A>G
ENST00000640374.1:n.263A>G
ENST00000640403.1:c.4410A>G	ENSP00000492531.1:p.Ile1470Met
ENST00000640779.1:c.1848A>G
ENST00000405460.6:c.7119A>G	ENSP00000384582.2:p.Ile2373Met
NM_032119.3:c.7119A>G	NP_115495.3:p.Ile2373Met
NR_003149.1:n.7132A>G
XM_011543675.1:c.7116A>G	XP_011541977.1:p.Ile2372Met
XM_011543676.1:c.7038A>G	XP_011541978.1:p.Ile2346Met
XM_011543677.1:c.4422A>G	XP_011541979.1:p.Ile1474Met
XM_011543678.1:c.7119A>G	XP_011541980.1:p.Ile2373Met
XM_011543679.1:c.7119A>G	XP_011541981.1:p.Ile2373Met
NM_032119.4:c.7119A>G MANE Select	NP_115495.3:p.Ile2373Met
XM_017009963.2:c.7119A>G	XP_016865452.1:p.Ile2373Met
XM_017009964.2:c.7116A>G	XP_016865453.1:p.Ile2372Met
XM_017009965.1:c.7116A>G	XP_016865454.1:p.Ile2372Met
XM_017009966.2:c.7038A>G	XP_016865455.1:p.Ile2346Met
XM_017009967.1:c.7023A>G	XP_016865456.1:p.Ile2341Met
XM_017009968.2:c.7119A>G	XP_016865457.1:p.Ile2373Met
XM_017009969.2:c.7119A>G	XP_016865458.1:p.Ile2373Met
XM_017009970.2:c.7119A>G	XP_016865459.1:p.Ile2373Met
XM_017009971.2:c.7119A>G	XP_016865460.1:p.Ile2373Met
XM_017009972.1:c.237A>G	XP_016865461.1:p.Ile79Met
XM_017009973.1:c.237A>G	XP_016865462.1:p.Ile79Met
XM_017009974.2:c.7119A>G	XP_016865463.1:p.Ile2373Met
NR_003149.2:n.7135A>G