Canonical Allele Identifier: CA445415754

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085560T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789743T>G , CM000667.2:g.90789743T>G	GRCh38
NC_000005.9:g.90085560T>G , CM000667.1:g.90085560T>G	GRCh37
NC_000005.8:g.90121316T>G	NCBI36
NG_007083.1:g.235944T>G
NG_007083.2:g.265400T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.13935T>G MANE Select	ENSP00000384582.2:p.Ala4645=
ENST00000425867.3:c.2889T>G	ENSP00000392618.3:p.Ala963=
ENST00000638510.1:n.1202T>G
ENST00000638975.1:c.564T>G	ENSP00000492630.1:p.Ala188=
ENST00000639431.1:c.265+113534T>G	ENSP00000491057.1:n.265+113534T>G
ENST00000640407.1:c.345T>G	ENSP00000491425.1:p.Ala115=
ENST00000405460.6:c.13935T>G	ENSP00000384582.2:p.Ala4645=
ENST00000425867.2:c.918T>G	ENSP00000392618.2:p.Ala306=
NM_032119.3:c.13935T>G	NP_115495.3:p.Ala4645=
NR_003149.1:n.13948T>G
XM_011543675.1:c.13932T>G	XP_011541977.1:p.Ala4644=
XM_011543676.1:c.13854T>G	XP_011541978.1:p.Ala4618=
XM_011543677.1:c.11238T>G	XP_011541979.1:p.Ala3746=
XM_011543678.1:c.13935T>G	XP_011541980.1:p.Ala4645=
NM_032119.4:c.13935T>G MANE Select	NP_115495.3:p.Ala4645=
XM_017009963.2:c.13956T>G	XP_016865452.1:p.Ala4652=
XM_017009964.2:c.13953T>G	XP_016865453.1:p.Ala4651=
XM_017009965.1:c.13953T>G	XP_016865454.1:p.Ala4651=
XM_017009966.2:c.13875T>G	XP_016865455.1:p.Ala4625=
XM_017009967.1:c.13860T>G	XP_016865456.1:p.Ala4620=
XM_017009968.2:c.13956T>G	XP_016865457.1:p.Ala4652=
XM_017009969.2:c.13956T>G	XP_016865458.1:p.Ala4652=
XM_017009970.2:c.13956T>G	XP_016865459.1:p.Ala4652=
XM_017009971.2:c.13956T>G	XP_016865460.1:p.Ala4652=
XM_017009972.1:c.7074T>G	XP_016865461.1:p.Ala2358=
XM_017009973.1:c.7053T>G	XP_016865462.1:p.Ala2351=
NR_003149.2:n.13951T>G