Canonical Allele Identifier: CA360409659

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90810732-A-G
• MyVariant Identifiers: chr5:g.90106549A>G (hg19) ; chr5:g.90810732A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810732A>G , CM000667.2:g.90810732A>G	GRCh38
NC_000005.9:g.90106549A>G , CM000667.1:g.90106549A>G	GRCh37
NC_000005.8:g.90142305A>G	NCBI36
NG_007083.1:g.256933A>G
NG_007083.2:g.286389A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15472A>G MANE Select	ENSP00000384582.2:p.Thr5158Ala
ENST00000425867.3:c.4426A>G	ENSP00000392618.3:p.Thr1476Ala
ENST00000638510.1:n.2739A>G
ENST00000639431.1:c.265+134523A>G	ENSP00000491057.1:n.265+134523A>G
ENST00000640407.1:c.1882A>G	ENSP00000491425.1:p.Thr628Ala
ENST00000405460.6:c.15472A>G	ENSP00000384582.2:p.Thr5158Ala
ENST00000425867.2:c.2455A>G	ENSP00000392618.2:p.Thr819Ala
NM_032119.3:c.15472A>G	NP_115495.3:p.Thr5158Ala
NR_003149.1:n.15485A>G
XM_011543675.1:c.15469A>G	XP_011541977.1:p.Thr5157Ala
XM_011543676.1:c.15391A>G	XP_011541978.1:p.Thr5131Ala
XM_011543677.1:c.12775A>G	XP_011541979.1:p.Thr4259Ala
NM_032119.4:c.15472A>G MANE Select	NP_115495.3:p.Thr5158Ala
XM_017009963.2:c.15493A>G	XP_016865452.1:p.Thr5165Ala
XM_017009964.2:c.15490A>G	XP_016865453.1:p.Thr5164Ala
XM_017009965.1:c.15490A>G	XP_016865454.1:p.Thr5164Ala
XM_017009966.2:c.15412A>G	XP_016865455.1:p.Thr5138Ala
XM_017009967.1:c.15397A>G	XP_016865456.1:p.Thr5133Ala
XM_017009968.2:c.15313A>G	XP_016865457.1:p.Thr5105Ala
XM_017009969.2:c.15493A>G	XP_016865458.1:p.Thr5165Ala
XM_017009971.2:c.*426A>G	XP_016865460.1:n.*426A>G
XM_017009972.1:c.8611A>G	XP_016865461.1:p.Thr2871Ala
XM_017009973.1:c.8590A>G	XP_016865462.1:p.Thr2864Ala
NR_003149.2:n.15488A>G