Canonical Allele Identifier: CA360429181

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985412C>G , CM000667.2:g.90985412C>G	GRCh38
NC_000005.9:g.90281229C>G , CM000667.1:g.90281229C>G	GRCh37
NC_000005.8:g.90316985C>G	NCBI36
NG_007083.1:g.431613C>G
NG_007083.2:g.461069C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18042C>G MANE Select	NP_115495.3:p.Phe6014Leu
ENST00000405460.9:c.18042C>G MANE Select	ENSP00000384582.2:p.Phe6014Leu
NM_032119.3:c.18042C>G	NP_115495.3:p.Phe6014Leu
NR_003149.1:n.18055C>G
NR_003149.2:n.18058C>G
ENST00000405460.6:c.18042C>G	ENSP00000384582.2:p.Phe6014Leu
ENST00000425867.2:c.5025C>G	ENSP00000392618.2:p.Phe1675Leu
ENST00000425867.3:c.6996C>G	ENSP00000392618.3:p.Phe2332Leu
ENST00000638510.1:n.5309C>G
ENST00000638990.1:c.1254C>G
ENST00000639431.1:c.334C>G	ENSP00000491057.1:n.334C>G
ENST00000639707.1:c.126C>G	ENSP00000492328.1:p.Phe42Leu
ENST00000639821.1:c.126C>G	ENSP00000492216.1:p.Phe42Leu
ENST00000640369.1:c.126C>G	ENSP00000491401.1:p.Phe42Leu
ENST00000640407.1:c.4491C>G	ENSP00000491425.1:n.4491C>G
ENST00000640815.1:c.126C>G	ENSP00000491767.1:p.Phe42Leu
XM_011543675.1:c.18039C>G	XP_011541977.1:p.Phe6013Leu
XM_011543676.1:c.17961C>G	XP_011541978.1:p.Phe5987Leu
XM_011543677.1:c.15345C>G	XP_011541979.1:p.Phe5115Leu
XM_017009963.2:c.18063C>G	XP_016865452.1:p.Phe6021Leu
XM_017009964.2:c.18060C>G	XP_016865453.1:p.Phe6020Leu
XM_017009965.1:c.18060C>G	XP_016865454.1:p.Phe6020Leu
XM_017009966.2:c.17982C>G	XP_016865455.1:p.Phe5994Leu
XM_017009967.1:c.17967C>G	XP_016865456.1:p.Phe5989Leu
XM_017009968.2:c.17883C>G	XP_016865457.1:p.Phe5961Leu
XM_017009969.2:c.18063C>G	XP_016865458.1:p.Phe6021Leu
XM_017009972.1:c.11181C>G	XP_016865461.1:p.Phe3727Leu
XM_017009973.1:c.11160C>G	XP_016865462.1:p.Phe3720Leu