Canonical Allele Identifier: CA3342512

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965538A>G , CM000667.2:g.90965538A>G	GRCh38
NC_000005.9:g.90261355A>G , CM000667.1:g.90261355A>G	GRCh37
NC_000005.8:g.90297111A>G	NCBI36
NG_007083.1:g.411739A>G
NG_007083.2:g.441195A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17973+7A>G MANE Select	NP_115495.3:n.17973+7A>G
ENST00000405460.9:c.17973+7A>G MANE Select	ENSP00000384582.2:n.17973+7A>G
NM_032119.3:c.17973+7A>G	NP_115495.3:n.17973+7A>G
NR_003149.1:n.17986+7A>G
NR_003149.2:n.17989+7A>G
ENST00000405460.6:c.17973+7A>G	ENSP00000384582.2:n.17973+7A>G
ENST00000425867.2:c.4956+7A>G	ENSP00000392618.2:n.4956+7A>G
ENST00000425867.3:c.6927+7A>G	ENSP00000392618.3:n.6927+7A>G
ENST00000638510.1:n.5240+7A>G
ENST00000638990.1:c.1185+7A>G
ENST00000639431.1:c.266-19806A>G	ENSP00000491057.1:n.266-19806A>G
ENST00000639707.1:c.57+7A>G	ENSP00000492328.1:n.57+7A>G
ENST00000639821.1:c.57+7A>G	ENSP00000492216.1:n.57+7A>G
ENST00000640369.1:c.57+7A>G	ENSP00000491401.1:n.57+7A>G
ENST00000640407.1:c.4422+7A>G	ENSP00000491425.1:n.4422+7A>G
ENST00000640815.1:c.57+7A>G	ENSP00000491767.1:n.57+7A>G
XM_011543675.1:c.17970+7A>G	XP_011541977.1:n.17970+7A>G
XM_011543676.1:c.17892+7A>G	XP_011541978.1:n.17892+7A>G
XM_011543677.1:c.15276+7A>G	XP_011541979.1:n.15276+7A>G
XM_017009963.2:c.17994+7A>G	XP_016865452.1:n.17994+7A>G
XM_017009964.2:c.17991+7A>G	XP_016865453.1:n.17991+7A>G
XM_017009965.1:c.17991+7A>G	XP_016865454.1:n.17991+7A>G
XM_017009966.2:c.17913+7A>G	XP_016865455.1:n.17913+7A>G
XM_017009967.1:c.17898+7A>G	XP_016865456.1:n.17898+7A>G
XM_017009968.2:c.17814+7A>G	XP_016865457.1:n.17814+7A>G
XM_017009969.2:c.17994+7A>G	XP_016865458.1:n.17994+7A>G
XM_017009972.1:c.11112+7A>G	XP_016865461.1:n.11112+7A>G
XM_017009973.1:c.11091+7A>G	XP_016865462.1:n.11091+7A>G