Canonical Allele Identifier: CA3341029

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90756598C>A , CM000667.2:g.90756598C>A	GRCh38
NC_000005.9:g.90052415C>A , CM000667.1:g.90052415C>A	GRCh37
NC_000005.8:g.90088171C>A	NCBI36
NG_007083.1:g.202799C>A
NG_007083.2:g.232255C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.11725C>A MANE Select	NP_115495.3:p.Pro3909Thr
ENST00000405460.9:c.11725C>A MANE Select	ENSP00000384582.2:p.Pro3909Thr
NM_032119.3:c.11725C>A	NP_115495.3:p.Pro3909Thr
NR_003149.1:n.11738C>A
NR_003149.2:n.11741C>A
ENST00000405460.6:c.11725C>A	ENSP00000384582.2:p.Pro3909Thr
ENST00000425867.3:c.712-381C>A	ENSP00000392618.3:n.712-381C>A
ENST00000509621.1:c.4422C>A
ENST00000639431.1:c.265+80389C>A	ENSP00000491057.1:n.265+80389C>A
ENST00000639884.1:n.31C>A
ENST00000640374.1:n.4725-381C>A
ENST00000640464.1:n.2144C>A
XM_011543675.1:c.11722C>A	XP_011541977.1:p.Pro3908Thr
XM_011543676.1:c.11644C>A	XP_011541978.1:p.Pro3882Thr
XM_011543677.1:c.9028C>A	XP_011541979.1:p.Pro3010Thr
XM_011543678.1:c.11725C>A	XP_011541980.1:p.Pro3909Thr
XM_017009963.2:c.11746C>A	XP_016865452.1:p.Pro3916Thr
XM_017009964.2:c.11743C>A	XP_016865453.1:p.Pro3915Thr
XM_017009965.1:c.11743C>A	XP_016865454.1:p.Pro3915Thr
XM_017009966.2:c.11665C>A	XP_016865455.1:p.Pro3889Thr
XM_017009967.1:c.11650C>A	XP_016865456.1:p.Pro3884Thr
XM_017009968.2:c.11746C>A	XP_016865457.1:p.Pro3916Thr
XM_017009969.2:c.11746C>A	XP_016865458.1:p.Pro3916Thr
XM_017009970.2:c.11746C>A	XP_016865459.1:p.Pro3916Thr
XM_017009971.2:c.11746C>A	XP_016865460.1:p.Pro3916Thr
XM_017009972.1:c.4864C>A	XP_016865461.1:p.Pro1622Thr
XM_017009973.1:c.4843C>A	XP_016865462.1:p.Pro1615Thr