Canonical Allele Identifier: CA360396980

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90788311G>A , CM000667.2:g.90788311G>A	GRCh38
NC_000005.9:g.90084128G>A , CM000667.1:g.90084128G>A	GRCh37
NC_000005.8:g.90119884G>A	NCBI36
NG_007083.1:g.234512G>A
NG_007083.2:g.263968G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13893+1G>A MANE Select	NP_115495.3:n.13893+1G>A
ENST00000405460.9:c.13893+1G>A MANE Select	ENSP00000384582.2:n.13893+1G>A
NM_032119.3:c.13893+1G>A	NP_115495.3:n.13893+1G>A
NR_003149.1:n.13906+1G>A
NR_003149.2:n.13909+1G>A
ENST00000405460.6:c.13893+1G>A	ENSP00000384582.2:n.13893+1G>A
ENST00000425867.2:c.876+1G>A	ENSP00000392618.2:n.876+1G>A
ENST00000425867.3:c.2847+1G>A	ENSP00000392618.3:n.2847+1G>A
ENST00000638510.1:n.1160+1G>A
ENST00000638975.1:c.522+1G>A	ENSP00000492630.1:n.522+1G>A
ENST00000639431.1:c.265+112102G>A	ENSP00000491057.1:n.265+112102G>A
ENST00000640407.1:c.303+1G>A	ENSP00000491425.1:n.303+1G>A
XM_011543675.1:c.13890+1G>A	XP_011541977.1:n.13890+1G>A
XM_011543676.1:c.13812+1G>A	XP_011541978.1:n.13812+1G>A
XM_011543677.1:c.11196+1G>A	XP_011541979.1:n.11196+1G>A
XM_011543678.1:c.13893+1G>A	XP_011541980.1:n.13893+1G>A
XM_017009963.2:c.13914+1G>A	XP_016865452.1:n.13914+1G>A
XM_017009964.2:c.13911+1G>A	XP_016865453.1:n.13911+1G>A
XM_017009965.1:c.13911+1G>A	XP_016865454.1:n.13911+1G>A
XM_017009966.2:c.13833+1G>A	XP_016865455.1:n.13833+1G>A
XM_017009967.1:c.13818+1G>A	XP_016865456.1:n.13818+1G>A
XM_017009968.2:c.13914+1G>A	XP_016865457.1:n.13914+1G>A
XM_017009969.2:c.13914+1G>A	XP_016865458.1:n.13914+1G>A
XM_017009970.2:c.13914+1G>A	XP_016865459.1:n.13914+1G>A
XM_017009971.2:c.13914+1G>A	XP_016865460.1:n.13914+1G>A
XM_017009972.1:c.7032+1G>A	XP_016865461.1:n.7032+1G>A
XM_017009973.1:c.7011+1G>A	XP_016865462.1:n.7011+1G>A