Canonical Allele Identifier: CA360401244

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90791102-A-G
• MyVariant Identifiers: chr5:g.90086919A>G (hg19) ; chr5:g.90791102A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791102A>G , CM000667.2:g.90791102A>G	GRCh38
NC_000005.9:g.90086919A>G , CM000667.1:g.90086919A>G	GRCh37
NC_000005.8:g.90122675A>G	NCBI36
NG_007083.1:g.237303A>G
NG_007083.2:g.266759A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14273A>G MANE Select	ENSP00000384582.2:p.Asp4758Gly
ENST00000425867.3:c.3227A>G	ENSP00000392618.3:p.Asp1076Gly
ENST00000638510.1:n.1540A>G
ENST00000638585.1:n.39A>G
ENST00000638975.1:c.902A>G	ENSP00000492630.1:p.Asp301Gly
ENST00000639431.1:c.265+114893A>G	ENSP00000491057.1:n.265+114893A>G
ENST00000640407.1:c.683A>G	ENSP00000491425.1:p.Asp228Gly
ENST00000405460.6:c.14273A>G	ENSP00000384582.2:p.Asp4758Gly
ENST00000425867.2:c.1256A>G	ENSP00000392618.2:p.Asp419Gly
NM_032119.3:c.14273A>G	NP_115495.3:p.Asp4758Gly
NR_003149.1:n.14286A>G
XM_011543675.1:c.14270A>G	XP_011541977.1:p.Asp4757Gly
XM_011543676.1:c.14192A>G	XP_011541978.1:p.Asp4731Gly
XM_011543677.1:c.11576A>G	XP_011541979.1:p.Asp3859Gly
XM_011543678.1:c.14273A>G	XP_011541980.1:p.Asp4758Gly
NM_032119.4:c.14273A>G MANE Select	NP_115495.3:p.Asp4758Gly
XM_017009963.2:c.14294A>G	XP_016865452.1:p.Asp4765Gly
XM_017009964.2:c.14291A>G	XP_016865453.1:p.Asp4764Gly
XM_017009965.1:c.14291A>G	XP_016865454.1:p.Asp4764Gly
XM_017009966.2:c.14213A>G	XP_016865455.1:p.Asp4738Gly
XM_017009967.1:c.14198A>G	XP_016865456.1:p.Asp4733Gly
XM_017009968.2:c.14294A>G	XP_016865457.1:p.Asp4765Gly
XM_017009969.2:c.14294A>G	XP_016865458.1:p.Asp4765Gly
XM_017009970.2:c.14294A>G	XP_016865459.1:p.Asp4765Gly
XM_017009971.2:c.14294A>G	XP_016865460.1:p.Asp4765Gly
XM_017009972.1:c.7412A>G	XP_016865461.1:p.Asp2471Gly
XM_017009973.1:c.7391A>G	XP_016865462.1:p.Asp2464Gly
NR_003149.2:n.14289A>G