Canonical Allele Identifier: CA445404513

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692688-T-C
• MyVariant Identifiers: chr5:g.89988505T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692688T>C , CM000667.2:g.90692688T>C	GRCh38
NC_000005.9:g.89988505T>C , CM000667.1:g.89988505T>C	GRCh37
NC_000005.8:g.90024261T>C	NCBI36
NG_007083.1:g.138889T>C
NG_007083.2:g.168345T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7035T>C MANE Select	ENSP00000384582.2:p.Asn2345=
ENST00000639431.1:c.265+16479T>C	ENSP00000491057.1:n.265+16479T>C
ENST00000639473.1:n.2494T>C
ENST00000640012.1:c.842T>C
ENST00000640374.1:n.179T>C
ENST00000640403.1:c.4326T>C	ENSP00000492531.1:p.Asn1442=
ENST00000640779.1:c.1764T>C
ENST00000405460.6:c.7035T>C	ENSP00000384582.2:p.Asn2345=
NM_032119.3:c.7035T>C	NP_115495.3:p.Asn2345=
NR_003149.1:n.7048T>C
XM_011543675.1:c.7032T>C	XP_011541977.1:p.Asn2344=
XM_011543676.1:c.6954T>C	XP_011541978.1:p.Asn2318=
XM_011543677.1:c.4338T>C	XP_011541979.1:p.Asn1446=
XM_011543678.1:c.7035T>C	XP_011541980.1:p.Asn2345=
XM_011543679.1:c.7035T>C	XP_011541981.1:p.Asn2345=
NM_032119.4:c.7035T>C MANE Select	NP_115495.3:p.Asn2345=
XM_017009963.2:c.7035T>C	XP_016865452.1:p.Asn2345=
XM_017009964.2:c.7032T>C	XP_016865453.1:p.Asn2344=
XM_017009965.1:c.7032T>C	XP_016865454.1:p.Asn2344=
XM_017009966.2:c.6954T>C	XP_016865455.1:p.Asn2318=
XM_017009967.1:c.6939T>C	XP_016865456.1:p.Asn2313=
XM_017009968.2:c.7035T>C	XP_016865457.1:p.Asn2345=
XM_017009969.2:c.7035T>C	XP_016865458.1:p.Asn2345=
XM_017009970.2:c.7035T>C	XP_016865459.1:p.Asn2345=
XM_017009971.2:c.7035T>C	XP_016865460.1:p.Asn2345=
XM_017009972.1:c.153T>C	XP_016865461.1:p.Asn51=
XM_017009973.1:c.153T>C	XP_016865462.1:p.Asn51=
XM_017009974.2:c.7035T>C	XP_016865463.1:p.Asn2345=
NR_003149.2:n.7051T>C