Canonical Allele Identifier: CA360413753

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683849T>G , CM000667.2:g.90683849T>G	GRCh38
NC_000005.9:g.89979666T>G , CM000667.1:g.89979666T>G	GRCh37
NC_000005.8:g.90015422T>G	NCBI36
NG_007083.1:g.130050T>G
NG_007083.2:g.159506T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5928T>G MANE Select	NP_115495.3:p.Tyr1976Ter
ENST00000405460.9:c.5928T>G MANE Select	ENSP00000384582.2:p.Tyr1976Ter
NM_032119.3:c.5928T>G	NP_115495.3:p.Tyr1976Ter
NR_003149.1:n.6024T>G
NR_003149.2:n.6027T>G
ENST00000405460.6:c.5928T>G	ENSP00000384582.2:p.Tyr1976Ter
ENST00000639431.1:c.265+7640T>G	ENSP00000491057.1:n.265+7640T>G
ENST00000639473.1:n.1387T>G
ENST00000640012.1:c.165-1931T>G
ENST00000640403.1:c.3219T>G	ENSP00000492531.1:p.Tyr1073Ter
ENST00000640779.1:c.740T>G
XM_011543675.1:c.5925T>G	XP_011541977.1:p.Tyr1975Ter
XM_011543676.1:c.5847T>G	XP_011541978.1:p.Tyr1949Ter
XM_011543677.1:c.3231T>G	XP_011541979.1:p.Tyr1077Ter
XM_011543678.1:c.5928T>G	XP_011541980.1:p.Tyr1976Ter
XM_011543679.1:c.5928T>G	XP_011541981.1:p.Tyr1976Ter
XM_017009963.2:c.5928T>G	XP_016865452.1:p.Tyr1976Ter
XM_017009964.2:c.5925T>G	XP_016865453.1:p.Tyr1975Ter
XM_017009965.1:c.5925T>G	XP_016865454.1:p.Tyr1975Ter
XM_017009966.2:c.5847T>G	XP_016865455.1:p.Tyr1949Ter
XM_017009967.1:c.5832T>G	XP_016865456.1:p.Tyr1944Ter
XM_017009968.2:c.5928T>G	XP_016865457.1:p.Tyr1976Ter
XM_017009969.2:c.5928T>G	XP_016865458.1:p.Tyr1976Ter
XM_017009970.2:c.5928T>G	XP_016865459.1:p.Tyr1976Ter
XM_017009971.2:c.5928T>G	XP_016865460.1:p.Tyr1976Ter
XM_017009973.1:c.-872T>G	XP_016865462.1:n.-872T>G
XM_017009974.2:c.5928T>G	XP_016865463.1:p.Tyr1976Ter