Canonical Allele Identifier: CA360409049

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041475A>G (hg19) ; chr5:g.90745658A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745658A>G , CM000667.2:g.90745658A>G	GRCh38
NC_000005.9:g.90041475A>G , CM000667.1:g.90041475A>G	GRCh37
NC_000005.8:g.90077231A>G	NCBI36
NG_007083.1:g.191859A>G
NG_007083.2:g.221315A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10837A>G MANE Select	ENSP00000384582.2:p.Thr3613Ala
ENST00000639431.1:c.265+69449A>G	ENSP00000491057.1:n.265+69449A>G
ENST00000640374.1:n.3981A>G
ENST00000640464.1:n.1256A>G
ENST00000405460.6:c.10837A>G	ENSP00000384582.2:p.Thr3613Ala
ENST00000509621.1:c.3534A>G
NM_032119.3:c.10837A>G	NP_115495.3:p.Thr3613Ala
NR_003149.1:n.10850A>G
XM_011543675.1:c.10834A>G	XP_011541977.1:p.Thr3612Ala
XM_011543676.1:c.10756A>G	XP_011541978.1:p.Thr3586Ala
XM_011543677.1:c.8140A>G	XP_011541979.1:p.Thr2714Ala
XM_011543678.1:c.10837A>G	XP_011541980.1:p.Thr3613Ala
XM_011543679.1:c.*59A>G	XP_011541981.1:n.*59A>G
NM_032119.4:c.10837A>G MANE Select	NP_115495.3:p.Thr3613Ala
XM_017009963.2:c.10858A>G	XP_016865452.1:p.Thr3620Ala
XM_017009964.2:c.10855A>G	XP_016865453.1:p.Thr3619Ala
XM_017009965.1:c.10855A>G	XP_016865454.1:p.Thr3619Ala
XM_017009966.2:c.10777A>G	XP_016865455.1:p.Thr3593Ala
XM_017009967.1:c.10762A>G	XP_016865456.1:p.Thr3588Ala
XM_017009968.2:c.10858A>G	XP_016865457.1:p.Thr3620Ala
XM_017009969.2:c.10858A>G	XP_016865458.1:p.Thr3620Ala
XM_017009970.2:c.10858A>G	XP_016865459.1:p.Thr3620Ala
XM_017009971.2:c.10858A>G	XP_016865460.1:p.Thr3620Ala
XM_017009972.1:c.3976A>G	XP_016865461.1:p.Thr1326Ala
XM_017009973.1:c.3955A>G	XP_016865462.1:p.Thr1319Ala
XM_017009974.2:c.*59A>G	XP_016865463.1:n.*59A>G
NR_003149.2:n.10853A>G