Canonical Allele Identifier: CA360390758

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1262040750
• gnomAD v4: 5-90644775-A-G
• MyVariant Identifiers: chr5:g.89940592A>G (hg19) ; chr5:g.90644775A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644775A>G , CM000667.2:g.90644775A>G	GRCh38
NC_000005.9:g.89940592A>G , CM000667.1:g.89940592A>G	GRCh37
NC_000005.8:g.89976348A>G	NCBI36
NG_007083.1:g.90976A>G
NG_007083.2:g.120432A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2804A>G MANE Select	ENSP00000384582.2:p.Asp935Gly
ENST00000504142.2:n.1570A>G
ENST00000639676.1:n.402A>G
ENST00000640403.1:c.107A>G	ENSP00000492531.1:p.Asp36Gly
ENST00000405460.6:c.2804A>G	ENSP00000384582.2:p.Asp935Gly
ENST00000504142.1:c.1569A>G
NM_032119.3:c.2804A>G	NP_115495.3:p.Asp935Gly
NR_003149.1:n.2900A>G
XM_011543675.1:c.2804A>G	XP_011541977.1:p.Asp935Gly
XM_011543676.1:c.2804A>G	XP_011541978.1:p.Asp935Gly
XM_011543677.1:c.107A>G	XP_011541979.1:p.Asp36Gly
XM_011543678.1:c.2804A>G	XP_011541980.1:p.Asp935Gly
XM_011543679.1:c.2804A>G	XP_011541981.1:p.Asp935Gly
NM_032119.4:c.2804A>G MANE Select	NP_115495.3:p.Asp935Gly
XM_017009963.2:c.2804A>G	XP_016865452.1:p.Asp935Gly
XM_017009964.2:c.2804A>G	XP_016865453.1:p.Asp935Gly
XM_017009965.1:c.2801A>G	XP_016865454.1:p.Asp934Gly
XM_017009966.2:c.2804A>G	XP_016865455.1:p.Asp935Gly
XM_017009967.1:c.2708A>G	XP_016865456.1:p.Asp903Gly
XM_017009968.2:c.2804A>G	XP_016865457.1:p.Asp935Gly
XM_017009969.2:c.2804A>G	XP_016865458.1:p.Asp935Gly
XM_017009970.2:c.2804A>G	XP_016865459.1:p.Asp935Gly
XM_017009971.2:c.2804A>G	XP_016865460.1:p.Asp935Gly
XM_017009974.2:c.2804A>G	XP_016865463.1:p.Asp935Gly
NR_003149.2:n.2903A>G