Canonical Allele Identifier: CA360403213

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021390A>G (hg19) ; chr5:g.90725573A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725573A>G , CM000667.2:g.90725573A>G	GRCh38
NC_000005.9:g.90021390A>G , CM000667.1:g.90021390A>G	GRCh37
NC_000005.8:g.90057146A>G	NCBI36
NG_007083.1:g.171774A>G
NG_007083.2:g.201230A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10078A>G MANE Select	ENSP00000384582.2:p.Ser3360Gly
ENST00000639431.1:c.265+49364A>G	ENSP00000491057.1:n.265+49364A>G
ENST00000640374.1:n.3222A>G
ENST00000640464.1:n.497A>G
ENST00000405460.6:c.10078A>G	ENSP00000384582.2:p.Ser3360Gly
ENST00000509621.1:c.2775A>G
NM_032119.3:c.10078A>G	NP_115495.3:p.Ser3360Gly
NR_003149.1:n.10091A>G
XM_011543675.1:c.10075A>G	XP_011541977.1:p.Ser3359Gly
XM_011543676.1:c.9997A>G	XP_011541978.1:p.Ser3333Gly
XM_011543677.1:c.7381A>G	XP_011541979.1:p.Ser2461Gly
XM_011543678.1:c.10078A>G	XP_011541980.1:p.Ser3360Gly
XM_011543679.1:c.10078A>G	XP_011541981.1:p.Ser3360Gly
XR_948560.1:n.272-9764T>C
NM_032119.4:c.10078A>G MANE Select	NP_115495.3:p.Ser3360Gly
XM_017009963.2:c.10099A>G	XP_016865452.1:p.Ser3367Gly
XM_017009964.2:c.10096A>G	XP_016865453.1:p.Ser3366Gly
XM_017009965.1:c.10096A>G	XP_016865454.1:p.Ser3366Gly
XM_017009966.2:c.10018A>G	XP_016865455.1:p.Ser3340Gly
XM_017009967.1:c.10003A>G	XP_016865456.1:p.Ser3335Gly
XM_017009968.2:c.10099A>G	XP_016865457.1:p.Ser3367Gly
XM_017009969.2:c.10099A>G	XP_016865458.1:p.Ser3367Gly
XM_017009970.2:c.10099A>G	XP_016865459.1:p.Ser3367Gly
XM_017009971.2:c.10099A>G	XP_016865460.1:p.Ser3367Gly
XM_017009972.1:c.3217A>G	XP_016865461.1:p.Ser1073Gly
XM_017009973.1:c.3196A>G	XP_016865462.1:p.Ser1066Gly
XM_017009974.2:c.10099A>G	XP_016865463.1:p.Ser3367Gly
XR_001742802.1:n.2523-9764T>C
NR_003149.2:n.10094A>G