Canonical Allele Identifier: CA445468349

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106551C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810734C>A , CM000667.2:g.90810734C>A	GRCh38
NC_000005.9:g.90106551C>A , CM000667.1:g.90106551C>A	GRCh37
NC_000005.8:g.90142307C>A	NCBI36
NG_007083.1:g.256935C>A
NG_007083.2:g.286391C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.15474C>A MANE Select	ENSP00000384582.2:p.Thr5158=
ENST00000425867.3:c.4428C>A	ENSP00000392618.3:p.Thr1476=
ENST00000638510.1:n.2741C>A
ENST00000639431.1:c.265+134525C>A	ENSP00000491057.1:n.265+134525C>A
ENST00000640407.1:c.1884C>A	ENSP00000491425.1:p.Thr628=
ENST00000405460.6:c.15474C>A	ENSP00000384582.2:p.Thr5158=
ENST00000425867.2:c.2457C>A	ENSP00000392618.2:p.Thr819=
NM_032119.3:c.15474C>A	NP_115495.3:p.Thr5158=
NR_003149.1:n.15487C>A
XM_011543675.1:c.15471C>A	XP_011541977.1:p.Thr5157=
XM_011543676.1:c.15393C>A	XP_011541978.1:p.Thr5131=
XM_011543677.1:c.12777C>A	XP_011541979.1:p.Thr4259=
NM_032119.4:c.15474C>A MANE Select	NP_115495.3:p.Thr5158=
XM_017009963.2:c.15495C>A	XP_016865452.1:p.Thr5165=
XM_017009964.2:c.15492C>A	XP_016865453.1:p.Thr5164=
XM_017009965.1:c.15492C>A	XP_016865454.1:p.Thr5164=
XM_017009966.2:c.15414C>A	XP_016865455.1:p.Thr5138=
XM_017009967.1:c.15399C>A	XP_016865456.1:p.Thr5133=
XM_017009968.2:c.15315C>A	XP_016865457.1:p.Thr5105=
XM_017009969.2:c.15495C>A	XP_016865458.1:p.Thr5165=
XM_017009971.2:c.*428C>A	XP_016865460.1:n.*428C>A
XM_017009972.1:c.8613C>A	XP_016865461.1:p.Thr2871=
XM_017009973.1:c.8592C>A	XP_016865462.1:p.Thr2864=
NR_003149.2:n.15490C>A