Canonical Allele Identifier: CA3342588

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91072475T>A , CM000667.2:g.91072475T>A	GRCh38
NC_000005.9:g.90368292T>A , CM000667.1:g.90368292T>A	GRCh37
NC_000005.8:g.90404048T>A	NCBI36
NG_007083.1:g.518676T>A
NG_007083.2:g.548132T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18181T>A MANE Select	NP_115495.3:p.Leu6061Met
ENST00000405460.9:c.18181T>A MANE Select	ENSP00000384582.2:p.Leu6061Met
NM_032119.3:c.18181T>A	NP_115495.3:p.Leu6061Met
NR_003149.1:n.18194T>A
NR_003149.2:n.18197T>A
ENST00000405460.6:c.18181T>A	ENSP00000384582.2:p.Leu6061Met
ENST00000425867.2:c.5164T>A	ENSP00000392618.2:p.Leu1722Met
ENST00000425867.3:c.7135T>A	ENSP00000392618.3:p.Leu2379Met
ENST00000638510.1:n.5448T>A
ENST00000638990.1:c.1393T>A
ENST00000639431.1:c.473T>A	ENSP00000491057.1:n.473T>A
ENST00000639707.1:c.265T>A	ENSP00000492328.1:p.Leu89Met
ENST00000639821.1:c.265T>A	ENSP00000492216.1:p.Leu89Met
ENST00000640369.1:c.265T>A	ENSP00000491401.1:p.Leu89Met
ENST00000640407.1:c.4630T>A	ENSP00000491425.1:n.4630T>A
ENST00000640815.1:c.265T>A	ENSP00000491767.1:p.Leu89Met
XM_011543675.1:c.18178T>A	XP_011541977.1:p.Leu6060Met
XM_011543676.1:c.18100T>A	XP_011541978.1:p.Leu6034Met
XM_011543677.1:c.15484T>A	XP_011541979.1:p.Leu5162Met
XM_017009963.2:c.18202T>A	XP_016865452.1:p.Leu6068Met
XM_017009964.2:c.18199T>A	XP_016865453.1:p.Leu6067Met
XM_017009965.1:c.18199T>A	XP_016865454.1:p.Leu6067Met
XM_017009966.2:c.18121T>A	XP_016865455.1:p.Leu6041Met
XM_017009967.1:c.18106T>A	XP_016865456.1:p.Leu6036Met
XM_017009968.2:c.18022T>A	XP_016865457.1:p.Leu6008Met
XM_017009969.2:c.18202T>A	XP_016865458.1:p.Leu6068Met
XM_017009972.1:c.11320T>A	XP_016865461.1:p.Leu3774Met
XM_017009973.1:c.11299T>A	XP_016865462.1:p.Leu3767Met