Canonical Allele Identifier: CA445467202

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979981T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684164T>G , CM000667.2:g.90684164T>G	GRCh38
NC_000005.9:g.89979981T>G , CM000667.1:g.89979981T>G	GRCh37
NC_000005.8:g.90015737T>G	NCBI36
NG_007083.1:g.130365T>G
NG_007083.2:g.159821T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6243T>G MANE Select	ENSP00000384582.2:p.Ser2081=
ENST00000639431.1:c.265+7955T>G	ENSP00000491057.1:n.265+7955T>G
ENST00000639473.1:n.1702T>G
ENST00000640012.1:c.165-1616T>G
ENST00000640403.1:c.3534T>G	ENSP00000492531.1:p.Ser1178=
ENST00000640779.1:c.1055T>G
ENST00000405460.6:c.6243T>G	ENSP00000384582.2:p.Ser2081=
NM_032119.3:c.6243T>G	NP_115495.3:p.Ser2081=
NR_003149.1:n.6339T>G
XM_011543675.1:c.6240T>G	XP_011541977.1:p.Ser2080=
XM_011543676.1:c.6162T>G	XP_011541978.1:p.Ser2054=
XM_011543677.1:c.3546T>G	XP_011541979.1:p.Ser1182=
XM_011543678.1:c.6243T>G	XP_011541980.1:p.Ser2081=
XM_011543679.1:c.6243T>G	XP_011541981.1:p.Ser2081=
NM_032119.4:c.6243T>G MANE Select	NP_115495.3:p.Ser2081=
XM_017009963.2:c.6243T>G	XP_016865452.1:p.Ser2081=
XM_017009964.2:c.6240T>G	XP_016865453.1:p.Ser2080=
XM_017009965.1:c.6240T>G	XP_016865454.1:p.Ser2080=
XM_017009966.2:c.6162T>G	XP_016865455.1:p.Ser2054=
XM_017009967.1:c.6147T>G	XP_016865456.1:p.Ser2049=
XM_017009968.2:c.6243T>G	XP_016865457.1:p.Ser2081=
XM_017009969.2:c.6243T>G	XP_016865458.1:p.Ser2081=
XM_017009970.2:c.6243T>G	XP_016865459.1:p.Ser2081=
XM_017009971.2:c.6243T>G	XP_016865460.1:p.Ser2081=
XM_017009973.1:c.-557T>G	XP_016865462.1:n.-557T>G
XM_017009974.2:c.6243T>G	XP_016865463.1:p.Ser2081=
NR_003149.2:n.6342T>G