Canonical Allele Identifier: CA561215832
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs989404511
gnomAD v2: 5-90209725-C-A
gnomAD v3: 5-90913908-C-A
gnomAD v4: 5-90913908-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90913908C>A , CM000667.2:g.90913908C>A GRCh38
NC_000005.9:g.90209725C>A , CM000667.1:g.90209725C>A GRCh37
NC_000005.8:g.90245481C>A NCBI36
NG_007083.1:g.360109C>A
NG_007083.2:g.389565C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.17856+50051C>A MANE Select ENSP00000384582.2:n.17856+50051C>A
ENST00000425867.3:c.6810+50051C>A ENSP00000392618.3:n.6810+50051C>A
ENST00000638510.1:n.5123+50051C>A
ENST00000638990.1:c.1068+50051C>A
ENST00000639431.1:c.266-71436C>A ENSP00000491057.1:n.266-71436C>A
ENST00000640407.1:c.4305+50051C>A ENSP00000491425.1:n.4305+50051C>A
ENST00000640815.1:c.-61+14585C>A ENSP00000491767.1:n.-61+14585C>A
ENST00000405460.6:c.17856+50051C>A ENSP00000384582.2:n.17856+50051C>A
ENST00000425867.2:c.4839+50051C>A ENSP00000392618.2:n.4839+50051C>A
NM_032119.3:c.17856+50051C>A NP_115495.3:n.17856+50051C>A
NR_003149.1:n.17869+50051C>A
XM_011543675.1:c.17853+50051C>A XP_011541977.1:n.17853+50051C>A
XM_011543676.1:c.17775+50051C>A XP_011541978.1:n.17775+50051C>A
XM_011543677.1:c.15159+50051C>A XP_011541979.1:n.15159+50051C>A
NM_032119.4:c.17856+50051C>A MANE Select NP_115495.3:n.17856+50051C>A
XM_017009963.2:c.17877+50051C>A XP_016865452.1:n.17877+50051C>A
XM_017009964.2:c.17874+50051C>A XP_016865453.1:n.17874+50051C>A
XM_017009965.1:c.17874+50051C>A XP_016865454.1:n.17874+50051C>A
XM_017009966.2:c.17796+50051C>A XP_016865455.1:n.17796+50051C>A
XM_017009967.1:c.17781+50051C>A XP_016865456.1:n.17781+50051C>A
XM_017009968.2:c.17697+50051C>A XP_016865457.1:n.17697+50051C>A
XM_017009969.2:c.17877+50051C>A XP_016865458.1:n.17877+50051C>A
XM_017009972.1:c.10995+50051C>A XP_016865461.1:n.10995+50051C>A
XM_017009973.1:c.10974+50051C>A XP_016865462.1:n.10974+50051C>A
NR_003149.2:n.17872+50051C>A