Canonical Allele Identifier: CA360401208

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086915A>C (hg19) ; chr5:g.90791098A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791098A>C , CM000667.2:g.90791098A>C	GRCh38
NC_000005.9:g.90086915A>C , CM000667.1:g.90086915A>C	GRCh37
NC_000005.8:g.90122671A>C	NCBI36
NG_007083.1:g.237299A>C
NG_007083.2:g.266755A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14269A>C MANE Select	ENSP00000384582.2:p.Asn4757His
ENST00000425867.3:c.3223A>C	ENSP00000392618.3:p.Asn1075His
ENST00000638510.1:n.1536A>C
ENST00000638585.1:n.35A>C
ENST00000638975.1:c.898A>C	ENSP00000492630.1:p.Asn300His
ENST00000639431.1:c.265+114889A>C	ENSP00000491057.1:n.265+114889A>C
ENST00000640407.1:c.679A>C	ENSP00000491425.1:p.Asn227His
ENST00000405460.6:c.14269A>C	ENSP00000384582.2:p.Asn4757His
ENST00000425867.2:c.1252A>C	ENSP00000392618.2:p.Asn418His
NM_032119.3:c.14269A>C	NP_115495.3:p.Asn4757His
NR_003149.1:n.14282A>C
XM_011543675.1:c.14266A>C	XP_011541977.1:p.Asn4756His
XM_011543676.1:c.14188A>C	XP_011541978.1:p.Asn4730His
XM_011543677.1:c.11572A>C	XP_011541979.1:p.Asn3858His
XM_011543678.1:c.14269A>C	XP_011541980.1:p.Asn4757His
NM_032119.4:c.14269A>C MANE Select	NP_115495.3:p.Asn4757His
XM_017009963.2:c.14290A>C	XP_016865452.1:p.Asn4764His
XM_017009964.2:c.14287A>C	XP_016865453.1:p.Asn4763His
XM_017009965.1:c.14287A>C	XP_016865454.1:p.Asn4763His
XM_017009966.2:c.14209A>C	XP_016865455.1:p.Asn4737His
XM_017009967.1:c.14194A>C	XP_016865456.1:p.Asn4732His
XM_017009968.2:c.14290A>C	XP_016865457.1:p.Asn4764His
XM_017009969.2:c.14290A>C	XP_016865458.1:p.Asn4764His
XM_017009970.2:c.14290A>C	XP_016865459.1:p.Asn4764His
XM_017009971.2:c.14290A>C	XP_016865460.1:p.Asn4764His
XM_017009972.1:c.7408A>C	XP_016865461.1:p.Asn2470His
XM_017009973.1:c.7387A>C	XP_016865462.1:p.Asn2463His
NR_003149.2:n.14285A>C