Canonical Allele Identifier: CA445416037

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1754535352
• gnomAD v3: 5-90745618-T-C
• gnomAD v4: 5-90745618-T-C
• MyVariant Identifiers: chr5:g.90041435T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745618T>C , CM000667.2:g.90745618T>C	GRCh38
NC_000005.9:g.90041435T>C , CM000667.1:g.90041435T>C	GRCh37
NC_000005.8:g.90077191T>C	NCBI36
NG_007083.1:g.191819T>C
NG_007083.2:g.221275T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10797T>C MANE Select	ENSP00000384582.2:p.Gly3599=
ENST00000639431.1:c.265+69409T>C	ENSP00000491057.1:n.265+69409T>C
ENST00000640374.1:n.3941T>C
ENST00000640464.1:n.1216T>C
ENST00000405460.6:c.10797T>C	ENSP00000384582.2:p.Gly3599=
ENST00000509621.1:c.3494T>C
NM_032119.3:c.10797T>C	NP_115495.3:p.Gly3599=
NR_003149.1:n.10810T>C
XM_011543675.1:c.10794T>C	XP_011541977.1:p.Gly3598=
XM_011543676.1:c.10716T>C	XP_011541978.1:p.Gly3572=
XM_011543677.1:c.8100T>C	XP_011541979.1:p.Gly2700=
XM_011543678.1:c.10797T>C	XP_011541980.1:p.Gly3599=
XM_011543679.1:c.*19T>C	XP_011541981.1:n.*19T>C
NM_032119.4:c.10797T>C MANE Select	NP_115495.3:p.Gly3599=
XM_017009963.2:c.10818T>C	XP_016865452.1:p.Gly3606=
XM_017009964.2:c.10815T>C	XP_016865453.1:p.Gly3605=
XM_017009965.1:c.10815T>C	XP_016865454.1:p.Gly3605=
XM_017009966.2:c.10737T>C	XP_016865455.1:p.Gly3579=
XM_017009967.1:c.10722T>C	XP_016865456.1:p.Gly3574=
XM_017009968.2:c.10818T>C	XP_016865457.1:p.Gly3606=
XM_017009969.2:c.10818T>C	XP_016865458.1:p.Gly3606=
XM_017009970.2:c.10818T>C	XP_016865459.1:p.Gly3606=
XM_017009971.2:c.10818T>C	XP_016865460.1:p.Gly3606=
XM_017009972.1:c.3936T>C	XP_016865461.1:p.Gly1312=
XM_017009973.1:c.3915T>C	XP_016865462.1:p.Gly1305=
XM_017009974.2:c.*19T>C	XP_016865463.1:n.*19T>C
NR_003149.2:n.10813T>C