Canonical Allele Identifier: CA176256

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90854135A>G , CM000667.2:g.90854135A>G	GRCh38
NC_000005.9:g.90149952A>G , CM000667.1:g.90149952A>G	GRCh37
NC_000005.8:g.90185708A>G	NCBI36
NG_007083.1:g.300336A>G
NG_007083.2:g.329792A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17528A>G MANE Select	NP_115495.3:p.Tyr5843Cys
ENST00000405460.9:c.17528A>G MANE Select	ENSP00000384582.2:p.Tyr5843Cys
NM_032119.3:c.17528A>G	NP_115495.3:p.Tyr5843Cys
NR_003149.1:n.17541A>G
NR_003149.2:n.17544A>G
ENST00000405460.6:c.17528A>G	ENSP00000384582.2:p.Tyr5843Cys
ENST00000425867.2:c.4511A>G	ENSP00000392618.2:p.Tyr1504Cys
ENST00000425867.3:c.6482A>G	ENSP00000392618.3:p.Tyr2161Cys
ENST00000503852.1:n.76A>G
ENST00000638510.1:n.4795A>G
ENST00000638990.1:c.740A>G
ENST00000639431.1:c.266-131209A>G	ENSP00000491057.1:n.266-131209A>G
ENST00000640407.1:c.3977A>G	ENSP00000491425.1:n.3977A>G
XM_011543675.1:c.17525A>G	XP_011541977.1:p.Tyr5842Cys
XM_011543676.1:c.17447A>G	XP_011541978.1:p.Tyr5816Cys
XM_011543677.1:c.14831A>G	XP_011541979.1:p.Tyr4944Cys
XM_017009963.2:c.17549A>G	XP_016865452.1:p.Tyr5850Cys
XM_017009964.2:c.17546A>G	XP_016865453.1:p.Tyr5849Cys
XM_017009965.1:c.17546A>G	XP_016865454.1:p.Tyr5849Cys
XM_017009966.2:c.17468A>G	XP_016865455.1:p.Tyr5823Cys
XM_017009967.1:c.17453A>G	XP_016865456.1:p.Tyr5818Cys
XM_017009968.2:c.17369A>G	XP_016865457.1:p.Tyr5790Cys
XM_017009969.2:c.17549A>G	XP_016865458.1:p.Tyr5850Cys
XM_017009972.1:c.10667A>G	XP_016865461.1:p.Tyr3556Cys
XM_017009973.1:c.10646A>G	XP_016865462.1:p.Tyr3549Cys