Canonical Allele Identifier: CA445404558

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988556A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692739A>G , CM000667.2:g.90692739A>G	GRCh38
NC_000005.9:g.89988556A>G , CM000667.1:g.89988556A>G	GRCh37
NC_000005.8:g.90024312A>G	NCBI36
NG_007083.1:g.138940A>G
NG_007083.2:g.168396A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7086A>G MANE Select	ENSP00000384582.2:p.Gln2362=
ENST00000639431.1:c.265+16530A>G	ENSP00000491057.1:n.265+16530A>G
ENST00000639473.1:n.2545A>G
ENST00000640012.1:c.893A>G
ENST00000640374.1:n.230A>G
ENST00000640403.1:c.4377A>G	ENSP00000492531.1:p.Gln1459=
ENST00000640779.1:c.1815A>G
ENST00000405460.6:c.7086A>G	ENSP00000384582.2:p.Gln2362=
NM_032119.3:c.7086A>G	NP_115495.3:p.Gln2362=
NR_003149.1:n.7099A>G
XM_011543675.1:c.7083A>G	XP_011541977.1:p.Gln2361=
XM_011543676.1:c.7005A>G	XP_011541978.1:p.Gln2335=
XM_011543677.1:c.4389A>G	XP_011541979.1:p.Gln1463=
XM_011543678.1:c.7086A>G	XP_011541980.1:p.Gln2362=
XM_011543679.1:c.7086A>G	XP_011541981.1:p.Gln2362=
NM_032119.4:c.7086A>G MANE Select	NP_115495.3:p.Gln2362=
XM_017009963.2:c.7086A>G	XP_016865452.1:p.Gln2362=
XM_017009964.2:c.7083A>G	XP_016865453.1:p.Gln2361=
XM_017009965.1:c.7083A>G	XP_016865454.1:p.Gln2361=
XM_017009966.2:c.7005A>G	XP_016865455.1:p.Gln2335=
XM_017009967.1:c.6990A>G	XP_016865456.1:p.Gln2330=
XM_017009968.2:c.7086A>G	XP_016865457.1:p.Gln2362=
XM_017009969.2:c.7086A>G	XP_016865458.1:p.Gln2362=
XM_017009970.2:c.7086A>G	XP_016865459.1:p.Gln2362=
XM_017009971.2:c.7086A>G	XP_016865460.1:p.Gln2362=
XM_017009972.1:c.204A>G	XP_016865461.1:p.Gln68=
XM_017009973.1:c.204A>G	XP_016865462.1:p.Gln68=
XM_017009974.2:c.7086A>G	XP_016865463.1:p.Gln2362=
NR_003149.2:n.7102A>G