Canonical Allele Identifier: CA445412014

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008202A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712385A>G , CM000667.2:g.90712385A>G	GRCh38
NC_000005.9:g.90008202A>G , CM000667.1:g.90008202A>G	GRCh37
NC_000005.8:g.90043958A>G	NCBI36
NG_007083.1:g.158586A>G
NG_007083.2:g.188042A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9141A>G MANE Select	ENSP00000384582.2:p.Leu3047=
ENST00000639431.1:c.265+36176A>G	ENSP00000491057.1:n.265+36176A>G
ENST00000639473.1:n.4600A>G
ENST00000640012.1:c.2948A>G
ENST00000640374.1:n.2285A>G
ENST00000640779.1:c.3870A>G
ENST00000405460.6:c.9141A>G	ENSP00000384582.2:p.Leu3047=
ENST00000509621.1:c.1838A>G
NM_032119.3:c.9141A>G	NP_115495.3:p.Leu3047=
NR_003149.1:n.9154A>G
XM_011543675.1:c.9138A>G	XP_011541977.1:p.Leu3046=
XM_011543676.1:c.9060A>G	XP_011541978.1:p.Leu3020=
XM_011543677.1:c.6444A>G	XP_011541979.1:p.Leu2148=
XM_011543678.1:c.9141A>G	XP_011541980.1:p.Leu3047=
XM_011543679.1:c.9141A>G	XP_011541981.1:p.Leu3047=
XR_948560.1:n.461T>C
NM_032119.4:c.9141A>G MANE Select	NP_115495.3:p.Leu3047=
XM_017009963.2:c.9162A>G	XP_016865452.1:p.Leu3054=
XM_017009964.2:c.9159A>G	XP_016865453.1:p.Leu3053=
XM_017009965.1:c.9159A>G	XP_016865454.1:p.Leu3053=
XM_017009966.2:c.9081A>G	XP_016865455.1:p.Leu3027=
XM_017009967.1:c.9066A>G	XP_016865456.1:p.Leu3022=
XM_017009968.2:c.9162A>G	XP_016865457.1:p.Leu3054=
XM_017009969.2:c.9162A>G	XP_016865458.1:p.Leu3054=
XM_017009970.2:c.9162A>G	XP_016865459.1:p.Leu3054=
XM_017009971.2:c.9162A>G	XP_016865460.1:p.Leu3054=
XM_017009972.1:c.2280A>G	XP_016865461.1:p.Leu760=
XM_017009973.1:c.2259A>G	XP_016865462.1:p.Leu753=
XM_017009974.2:c.9162A>G	XP_016865463.1:p.Leu3054=
NR_003149.2:n.9157A>G