Canonical Allele Identifier: CA360363726

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90622702G>T , CM000667.2:g.90622702G>T	GRCh38
NC_000005.9:g.89918519G>T , CM000667.1:g.89918519G>T	GRCh37
NC_000005.8:g.89954275G>T	NCBI36
NG_007083.1:g.68903G>T
NG_007083.2:g.98359G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.558+1G>T MANE Select	NP_115495.3:n.558+1G>T
ENST00000405460.9:c.558+1G>T MANE Select	ENSP00000384582.2:n.558+1G>T
NM_032119.3:c.558+1G>T	NP_115495.3:n.558+1G>T
NR_003149.1:n.654+1G>T
NR_003149.2:n.657+1G>T
ENST00000405460.6:c.558+1G>T	ENSP00000384582.2:n.558+1G>T
ENST00000638316.1:n.768+1G>T
ENST00000638638.1:n.965+1G>T
ENST00000640083.1:n.263+1G>T
ENST00000640109.1:n.654+1G>T
ENST00000640281.1:n.617+1G>T
XM_011543675.1:c.558+1G>T	XP_011541977.1:n.558+1G>T
XM_011543676.1:c.558+1G>T	XP_011541978.1:n.558+1G>T
XM_011543678.1:c.558+1G>T	XP_011541980.1:n.558+1G>T
XM_011543679.1:c.558+1G>T	XP_011541981.1:n.558+1G>T
XM_017009963.2:c.558+1G>T	XP_016865452.1:n.558+1G>T
XM_017009964.2:c.558+1G>T	XP_016865453.1:n.558+1G>T
XM_017009965.1:c.555+1G>T	XP_016865454.1:n.555+1G>T
XM_017009966.2:c.558+1G>T	XP_016865455.1:n.558+1G>T
XM_017009967.1:c.462+1G>T	XP_016865456.1:n.462+1G>T
XM_017009968.2:c.558+1G>T	XP_016865457.1:n.558+1G>T
XM_017009969.2:c.558+1G>T	XP_016865458.1:n.558+1G>T
XM_017009970.2:c.558+1G>T	XP_016865459.1:n.558+1G>T
XM_017009971.2:c.558+1G>T	XP_016865460.1:n.558+1G>T
XM_017009974.2:c.558+1G>T	XP_016865463.1:n.558+1G>T