Canonical Allele Identifier: CA1078673086

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1773113829
• gnomAD v3: 5-90913832-T-G
• gnomAD v4: 5-90913832-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90913832T>G , CM000667.2:g.90913832T>G	GRCh38
NC_000005.9:g.90209649T>G , CM000667.1:g.90209649T>G	GRCh37
NC_000005.8:g.90245405T>G	NCBI36
NG_007083.1:g.360033T>G
NG_007083.2:g.389489T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17856+49975T>G MANE Select	ENSP00000384582.2:n.17856+49975T>G
ENST00000425867.3:c.6810+49975T>G	ENSP00000392618.3:n.6810+49975T>G
ENST00000638510.1:n.5123+49975T>G
ENST00000638990.1:c.1068+49975T>G
ENST00000639431.1:c.266-71512T>G	ENSP00000491057.1:n.266-71512T>G
ENST00000640407.1:c.4305+49975T>G	ENSP00000491425.1:n.4305+49975T>G
ENST00000640815.1:c.-61+14509T>G	ENSP00000491767.1:n.-61+14509T>G
ENST00000405460.6:c.17856+49975T>G	ENSP00000384582.2:n.17856+49975T>G
ENST00000425867.2:c.4839+49975T>G	ENSP00000392618.2:n.4839+49975T>G
NM_032119.3:c.17856+49975T>G	NP_115495.3:n.17856+49975T>G
NR_003149.1:n.17869+49975T>G
XM_011543675.1:c.17853+49975T>G	XP_011541977.1:n.17853+49975T>G
XM_011543676.1:c.17775+49975T>G	XP_011541978.1:n.17775+49975T>G
XM_011543677.1:c.15159+49975T>G	XP_011541979.1:n.15159+49975T>G
NM_032119.4:c.17856+49975T>G MANE Select	NP_115495.3:n.17856+49975T>G
XM_017009963.2:c.17877+49975T>G	XP_016865452.1:n.17877+49975T>G
XM_017009964.2:c.17874+49975T>G	XP_016865453.1:n.17874+49975T>G
XM_017009965.1:c.17874+49975T>G	XP_016865454.1:n.17874+49975T>G
XM_017009966.2:c.17796+49975T>G	XP_016865455.1:n.17796+49975T>G
XM_017009967.1:c.17781+49975T>G	XP_016865456.1:n.17781+49975T>G
XM_017009968.2:c.17697+49975T>G	XP_016865457.1:n.17697+49975T>G
XM_017009969.2:c.17877+49975T>G	XP_016865458.1:n.17877+49975T>G
XM_017009972.1:c.10995+49975T>G	XP_016865461.1:n.10995+49975T>G
XM_017009973.1:c.10974+49975T>G	XP_016865462.1:n.10974+49975T>G
NR_003149.2:n.17872+49975T>G