Canonical Allele Identifier: CA1562956722

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90913908_90913912delinsCGGGT , CM000667.2:g.90913908_90913912delinsCGGGT	GRCh38
NC_000005.9:g.90209725_90209729delinsCGGGT , CM000667.1:g.90209725_90209729delinsCGGGT	GRCh37
NC_000005.8:g.90245481_90245485delinsCGGGT	NCBI36
NG_007083.1:g.360109_360113delinsCGGGT
NG_007083.2:g.389565_389569delinsCGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.17856+50051_17856+50055delinsCGGGT MANE Select	ENSP00000384582.2:n.17856+50051_17856+50055delinsCGGGT
ENST00000425867.3:c.6810+50051_6810+50055delinsCGGGT	ENSP00000392618.3:n.6810+50051_6810+50055delinsCGGGT
ENST00000638510.1:n.5123+50051_5123+50055delinsCGGGT
ENST00000638990.1:c.1068+50051_1068+50055delinsCGGGT
ENST00000639431.1:c.266-71436_266-71432delinsCGGGT	ENSP00000491057.1:n.266-71436_266-71432delinsCGGGT
ENST00000640407.1:c.4305+50051_4305+50055delinsCGGGT	ENSP00000491425.1:n.4305+50051_4305+50055delinsCGGGT
ENST00000640815.1:c.-61+14585_-61+14589delinsCGGGT	ENSP00000491767.1:n.-61+14585_-61+14589delinsCGGGT
ENST00000405460.6:c.17856+50051_17856+50055delinsCGGGT	ENSP00000384582.2:n.17856+50051_17856+50055delinsCGGGT
ENST00000425867.2:c.4839+50051_4839+50055delinsCGGGT	ENSP00000392618.2:n.4839+50051_4839+50055delinsCGGGT
NM_032119.3:c.17856+50051_17856+50055delinsCGGGT	NP_115495.3:n.17856+50051_17856+50055delinsCGGGT
NR_003149.1:n.17869+50051_17869+50055delinsCGGGT
XM_011543675.1:c.17853+50051_17853+50055delinsCGGGT	XP_011541977.1:n.17853+50051_17853+50055delinsCGGGT
XM_011543676.1:c.17775+50051_17775+50055delinsCGGGT	XP_011541978.1:n.17775+50051_17775+50055delinsCGGGT
XM_011543677.1:c.15159+50051_15159+50055delinsCGGGT	XP_011541979.1:n.15159+50051_15159+50055delinsCGGGT
NM_032119.4:c.17856+50051_17856+50055delinsCGGGT MANE Select	NP_115495.3:n.17856+50051_17856+50055delinsCGGGT
XM_017009963.2:c.17877+50051_17877+50055delinsCGGGT	XP_016865452.1:n.17877+50051_17877+50055delinsCGGGT
XM_017009964.2:c.17874+50051_17874+50055delinsCGGGT	XP_016865453.1:n.17874+50051_17874+50055delinsCGGGT
XM_017009965.1:c.17874+50051_17874+50055delinsCGGGT	XP_016865454.1:n.17874+50051_17874+50055delinsCGGGT
XM_017009966.2:c.17796+50051_17796+50055delinsCGGGT	XP_016865455.1:n.17796+50051_17796+50055delinsCGGGT
XM_017009967.1:c.17781+50051_17781+50055delinsCGGGT	XP_016865456.1:n.17781+50051_17781+50055delinsCGGGT
XM_017009968.2:c.17697+50051_17697+50055delinsCGGGT	XP_016865457.1:n.17697+50051_17697+50055delinsCGGGT
XM_017009969.2:c.17877+50051_17877+50055delinsCGGGT	XP_016865458.1:n.17877+50051_17877+50055delinsCGGGT
XM_017009972.1:c.10995+50051_10995+50055delinsCGGGT	XP_016865461.1:n.10995+50051_10995+50055delinsCGGGT
XM_017009973.1:c.10974+50051_10974+50055delinsCGGGT	XP_016865462.1:n.10974+50051_10974+50055delinsCGGGT
NR_003149.2:n.17872+50051_17872+50055delinsCGGGT