Canonical Allele Identifier: CA176254

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90853421A>G , CM000667.2:g.90853421A>G	GRCh38
NC_000005.9:g.90149238A>G , CM000667.1:g.90149238A>G	GRCh37
NC_000005.8:g.90184994A>G	NCBI36
NG_007083.1:g.299622A>G
NG_007083.2:g.329078A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17342A>G MANE Select	NP_115495.3:p.Gln5781Arg
ENST00000405460.9:c.17342A>G MANE Select	ENSP00000384582.2:p.Gln5781Arg
NM_032119.3:c.17342A>G	NP_115495.3:p.Gln5781Arg
NR_003149.1:n.17355A>G
NR_003149.2:n.17358A>G
ENST00000405460.6:c.17342A>G	ENSP00000384582.2:p.Gln5781Arg
ENST00000425867.2:c.4325A>G	ENSP00000392618.2:p.Gln1442Arg
ENST00000425867.3:c.6296A>G	ENSP00000392618.3:p.Gln2099Arg
ENST00000505845.2:n.533A>G
ENST00000638510.1:n.4609A>G
ENST00000638990.1:c.554A>G
ENST00000639431.1:c.266-131923A>G	ENSP00000491057.1:n.266-131923A>G
ENST00000640407.1:c.3791A>G	ENSP00000491425.1:n.3791A>G
XM_011543675.1:c.17339A>G	XP_011541977.1:p.Gln5780Arg
XM_011543676.1:c.17261A>G	XP_011541978.1:p.Gln5754Arg
XM_011543677.1:c.14645A>G	XP_011541979.1:p.Gln4882Arg
XM_017009963.2:c.17363A>G	XP_016865452.1:p.Gln5788Arg
XM_017009964.2:c.17360A>G	XP_016865453.1:p.Gln5787Arg
XM_017009965.1:c.17360A>G	XP_016865454.1:p.Gln5787Arg
XM_017009966.2:c.17282A>G	XP_016865455.1:p.Gln5761Arg
XM_017009967.1:c.17267A>G	XP_016865456.1:p.Gln5756Arg
XM_017009968.2:c.17183A>G	XP_016865457.1:p.Gln5728Arg
XM_017009969.2:c.17363A>G	XP_016865458.1:p.Gln5788Arg
XM_017009972.1:c.10481A>G	XP_016865461.1:p.Gln3494Arg
XM_017009973.1:c.10460A>G	XP_016865462.1:p.Gln3487Arg