Canonical Allele Identifier: CA360407465

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1484688327
• gnomAD v3: 5-90745060-A-C
• gnomAD v4: 5-90745060-A-C
• MyVariant Identifiers: chr5:g.90040877A>C (hg19) ; chr5:g.90745060A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745060A>C , CM000667.2:g.90745060A>C	GRCh38
NC_000005.9:g.90040877A>C , CM000667.1:g.90040877A>C	GRCh37
NC_000005.8:g.90076633A>C	NCBI36
NG_007083.1:g.191261A>C
NG_007083.2:g.220717A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10564A>C MANE Select	ENSP00000384582.2:p.Ile3522Leu
ENST00000639431.1:c.265+68851A>C	ENSP00000491057.1:n.265+68851A>C
ENST00000640374.1:n.3708A>C
ENST00000640464.1:n.983A>C
ENST00000405460.6:c.10564A>C	ENSP00000384582.2:p.Ile3522Leu
ENST00000509621.1:c.3261A>C
NM_032119.3:c.10564A>C	NP_115495.3:p.Ile3522Leu
NR_003149.1:n.10577A>C
XM_011543675.1:c.10561A>C	XP_011541977.1:p.Ile3521Leu
XM_011543676.1:c.10483A>C	XP_011541978.1:p.Ile3495Leu
XM_011543677.1:c.7867A>C	XP_011541979.1:p.Ile2623Leu
XM_011543678.1:c.10564A>C	XP_011541980.1:p.Ile3522Leu
XM_011543679.1:c.10564A>C	XP_011541981.1:p.Ile3522Leu
NM_032119.4:c.10564A>C MANE Select	NP_115495.3:p.Ile3522Leu
XM_017009963.2:c.10585A>C	XP_016865452.1:p.Ile3529Leu
XM_017009964.2:c.10582A>C	XP_016865453.1:p.Ile3528Leu
XM_017009965.1:c.10582A>C	XP_016865454.1:p.Ile3528Leu
XM_017009966.2:c.10504A>C	XP_016865455.1:p.Ile3502Leu
XM_017009967.1:c.10489A>C	XP_016865456.1:p.Ile3497Leu
XM_017009968.2:c.10585A>C	XP_016865457.1:p.Ile3529Leu
XM_017009969.2:c.10585A>C	XP_016865458.1:p.Ile3529Leu
XM_017009970.2:c.10585A>C	XP_016865459.1:p.Ile3529Leu
XM_017009971.2:c.10585A>C	XP_016865460.1:p.Ile3529Leu
XM_017009972.1:c.3703A>C	XP_016865461.1:p.Ile1235Leu
XM_017009973.1:c.3682A>C	XP_016865462.1:p.Ile1228Leu
XM_017009974.2:c.10585A>C	XP_016865463.1:p.Ile3529Leu
NR_003149.2:n.10580A>C