Canonical Allele Identifier: CA360425491

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119265T>G (hg19) ; chr5:g.90823448T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823448T>G , CM000667.2:g.90823448T>G	GRCh38
NC_000005.9:g.90119265T>G , CM000667.1:g.90119265T>G	GRCh37
NC_000005.8:g.90155021T>G	NCBI36
NG_007083.1:g.269649T>G
NG_007083.2:g.299105T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16220T>G MANE Select	ENSP00000384582.2:p.Phe5407Cys
ENST00000425867.3:c.5174T>G	ENSP00000392618.3:p.Phe1725Cys
ENST00000638510.1:n.3487T>G
ENST00000639431.1:c.265+147239T>G	ENSP00000491057.1:n.265+147239T>G
ENST00000640061.1:n.128+1266T>G
ENST00000640407.1:c.2630T>G	ENSP00000491425.1:p.Phe877Cys
ENST00000405460.6:c.16220T>G	ENSP00000384582.2:p.Phe5407Cys
ENST00000425867.2:c.3203T>G	ENSP00000392618.2:p.Phe1068Cys
NM_032119.3:c.16220T>G	NP_115495.3:p.Phe5407Cys
NR_003149.1:n.16233T>G
XM_011543675.1:c.16217T>G	XP_011541977.1:p.Phe5406Cys
XM_011543676.1:c.16139T>G	XP_011541978.1:p.Phe5380Cys
XM_011543677.1:c.13523T>G	XP_011541979.1:p.Phe4508Cys
NM_032119.4:c.16220T>G MANE Select	NP_115495.3:p.Phe5407Cys
XM_017009963.2:c.16241T>G	XP_016865452.1:p.Phe5414Cys
XM_017009964.2:c.16238T>G	XP_016865453.1:p.Phe5413Cys
XM_017009965.1:c.16238T>G	XP_016865454.1:p.Phe5413Cys
XM_017009966.2:c.16160T>G	XP_016865455.1:p.Phe5387Cys
XM_017009967.1:c.16145T>G	XP_016865456.1:p.Phe5382Cys
XM_017009968.2:c.16061T>G	XP_016865457.1:p.Phe5354Cys
XM_017009969.2:c.16241T>G	XP_016865458.1:p.Phe5414Cys
XM_017009972.1:c.9359T>G	XP_016865461.1:p.Phe3120Cys
XM_017009973.1:c.9338T>G	XP_016865462.1:p.Phe3113Cys
NR_003149.2:n.16236T>G