Canonical Allele Identifier: CA360425663

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119355C>G (hg19) ; chr5:g.90823538C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823538C>G , CM000667.2:g.90823538C>G	GRCh38
NC_000005.9:g.90119355C>G , CM000667.1:g.90119355C>G	GRCh37
NC_000005.8:g.90155111C>G	NCBI36
NG_007083.1:g.269739C>G
NG_007083.2:g.299195C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16310C>G MANE Select	ENSP00000384582.2:p.Thr5437Arg
ENST00000425867.3:c.5264C>G	ENSP00000392618.3:p.Thr1755Arg
ENST00000638510.1:n.3577C>G
ENST00000639431.1:c.265+147329C>G	ENSP00000491057.1:n.265+147329C>G
ENST00000640061.1:n.128+1356C>G
ENST00000640407.1:c.2720C>G	ENSP00000491425.1:p.Thr907Arg
ENST00000405460.6:c.16310C>G	ENSP00000384582.2:p.Thr5437Arg
ENST00000425867.2:c.3293C>G	ENSP00000392618.2:p.Thr1098Arg
NM_032119.3:c.16310C>G	NP_115495.3:p.Thr5437Arg
NR_003149.1:n.16323C>G
XM_011543675.1:c.16307C>G	XP_011541977.1:p.Thr5436Arg
XM_011543676.1:c.16229C>G	XP_011541978.1:p.Thr5410Arg
XM_011543677.1:c.13613C>G	XP_011541979.1:p.Thr4538Arg
NM_032119.4:c.16310C>G MANE Select	NP_115495.3:p.Thr5437Arg
XM_017009963.2:c.16331C>G	XP_016865452.1:p.Thr5444Arg
XM_017009964.2:c.16328C>G	XP_016865453.1:p.Thr5443Arg
XM_017009965.1:c.16328C>G	XP_016865454.1:p.Thr5443Arg
XM_017009966.2:c.16250C>G	XP_016865455.1:p.Thr5417Arg
XM_017009967.1:c.16235C>G	XP_016865456.1:p.Thr5412Arg
XM_017009968.2:c.16151C>G	XP_016865457.1:p.Thr5384Arg
XM_017009969.2:c.16331C>G	XP_016865458.1:p.Thr5444Arg
XM_017009972.1:c.9449C>G	XP_016865461.1:p.Thr3150Arg
XM_017009973.1:c.9428C>G	XP_016865462.1:p.Thr3143Arg
NR_003149.2:n.16326C>G