Canonical Allele Identifier: CA2767415156

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617991_90617992insA , CM000667.2:g.90617991_90617992insA	GRCh38
NC_000005.9:g.89913808_89913809insA , CM000667.1:g.89913808_89913809insA	GRCh37
NC_000005.8:g.89949564_89949565insA	NCBI36
NG_007083.1:g.64192_64193insA
NG_007083.2:g.93648_93649insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.357+38_357+39insA MANE Select	ENSP00000384582.2:n.357+38_357+39insA
ENST00000638316.1:n.567+38_567+39insA
ENST00000638638.1:n.764+38_764+39insA
ENST00000640083.1:n.62+38_62+39insA
ENST00000640109.1:n.453+38_453+39insA
ENST00000640281.1:n.416+38_416+39insA
ENST00000405460.6:c.357+38_357+39insA	ENSP00000384582.2:n.357+38_357+39insA
ENST00000508842.5:c.369+38_369+39insA	ENSP00000425936.1:n.369+38_369+39insA
NM_032119.3:c.357+38_357+39insA	NP_115495.3:n.357+38_357+39insA
NR_003149.1:n.453+38_453+39insA
XM_011543675.1:c.357+38_357+39insA	XP_011541977.1:n.357+38_357+39insA
XM_011543676.1:c.357+38_357+39insA	XP_011541978.1:n.357+38_357+39insA
XM_011543678.1:c.357+38_357+39insA	XP_011541980.1:n.357+38_357+39insA
XM_011543679.1:c.357+38_357+39insA	XP_011541981.1:n.357+38_357+39insA
NM_032119.4:c.357+38_357+39insA MANE Select	NP_115495.3:n.357+38_357+39insA
XM_017009963.2:c.357+38_357+39insA	XP_016865452.1:n.357+38_357+39insA
XM_017009964.2:c.357+38_357+39insA	XP_016865453.1:n.357+38_357+39insA
XM_017009965.1:c.354+38_354+39insA	XP_016865454.1:n.354+38_354+39insA
XM_017009966.2:c.357+38_357+39insA	XP_016865455.1:n.357+38_357+39insA
XM_017009967.1:c.357+38_357+39insA	XP_016865456.1:n.357+38_357+39insA
XM_017009968.2:c.357+38_357+39insA	XP_016865457.1:n.357+38_357+39insA
XM_017009969.2:c.357+38_357+39insA	XP_016865458.1:n.357+38_357+39insA
XM_017009970.2:c.357+38_357+39insA	XP_016865459.1:n.357+38_357+39insA
XM_017009971.2:c.357+38_357+39insA	XP_016865460.1:n.357+38_357+39insA
XM_017009974.2:c.357+38_357+39insA	XP_016865463.1:n.357+38_357+39insA
NR_003149.2:n.456+38_456+39insA