Canonical Allele Identifier: CA122800401

Gene: ADGRV1

Linked Data

• dbSNP Id: rs543546393
• gnomAD v3: 5-90763415-T-C
• gnomAD v4: 5-90763415-T-C
• MyVariant Identifiers: chr5:g.90059232T>C (hg19) ; chr5:g.90763415T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763415T>C , CM000667.2:g.90763415T>C	GRCh38
NC_000005.9:g.90059232T>C , CM000667.1:g.90059232T>C	GRCh37
NC_000005.8:g.90094988T>C	NCBI36
NG_007083.1:g.209616T>C
NG_007083.2:g.239072T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12231T>C MANE Select	ENSP00000384582.2:p.Asp4077=
ENST00000425867.3:c.1185T>C	ENSP00000392618.3:p.Asp395=
ENST00000639431.1:c.265+87206T>C	ENSP00000491057.1:n.265+87206T>C
ENST00000640464.1:n.2650T>C
ENST00000640729.1:n.808T>C
ENST00000405460.6:c.12231T>C	ENSP00000384582.2:p.Asp4077=
NM_032119.3:c.12231T>C	NP_115495.3:p.Asp4077=
NR_003149.1:n.12244T>C
XM_011543675.1:c.12228T>C	XP_011541977.1:p.Asp4076=
XM_011543676.1:c.12150T>C	XP_011541978.1:p.Asp4050=
XM_011543677.1:c.9534T>C	XP_011541979.1:p.Asp3178=
XM_011543678.1:c.12231T>C	XP_011541980.1:p.Asp4077=
NM_032119.4:c.12231T>C MANE Select	NP_115495.3:p.Asp4077=
XM_017009963.2:c.12252T>C	XP_016865452.1:p.Asp4084=
XM_017009964.2:c.12249T>C	XP_016865453.1:p.Asp4083=
XM_017009965.1:c.12249T>C	XP_016865454.1:p.Asp4083=
XM_017009966.2:c.12171T>C	XP_016865455.1:p.Asp4057=
XM_017009967.1:c.12156T>C	XP_016865456.1:p.Asp4052=
XM_017009968.2:c.12252T>C	XP_016865457.1:p.Asp4084=
XM_017009969.2:c.12252T>C	XP_016865458.1:p.Asp4084=
XM_017009970.2:c.12252T>C	XP_016865459.1:p.Asp4084=
XM_017009971.2:c.12252T>C	XP_016865460.1:p.Asp4084=
XM_017009972.1:c.5370T>C	XP_016865461.1:p.Asp1790=
XM_017009973.1:c.5349T>C	XP_016865462.1:p.Asp1783=
NR_003149.2:n.12247T>C