Canonical Allele Identifier: CA445404533

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988532T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692715T>C , CM000667.2:g.90692715T>C	GRCh38
NC_000005.9:g.89988532T>C , CM000667.1:g.89988532T>C	GRCh37
NC_000005.8:g.90024288T>C	NCBI36
NG_007083.1:g.138916T>C
NG_007083.2:g.168372T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7062T>C MANE Select	ENSP00000384582.2:p.Phe2354=
ENST00000639431.1:c.265+16506T>C	ENSP00000491057.1:n.265+16506T>C
ENST00000639473.1:n.2521T>C
ENST00000640012.1:c.869T>C
ENST00000640374.1:n.206T>C
ENST00000640403.1:c.4353T>C	ENSP00000492531.1:p.Phe1451=
ENST00000640779.1:c.1791T>C
ENST00000405460.6:c.7062T>C	ENSP00000384582.2:p.Phe2354=
NM_032119.3:c.7062T>C	NP_115495.3:p.Phe2354=
NR_003149.1:n.7075T>C
XM_011543675.1:c.7059T>C	XP_011541977.1:p.Phe2353=
XM_011543676.1:c.6981T>C	XP_011541978.1:p.Phe2327=
XM_011543677.1:c.4365T>C	XP_011541979.1:p.Phe1455=
XM_011543678.1:c.7062T>C	XP_011541980.1:p.Phe2354=
XM_011543679.1:c.7062T>C	XP_011541981.1:p.Phe2354=
NM_032119.4:c.7062T>C MANE Select	NP_115495.3:p.Phe2354=
XM_017009963.2:c.7062T>C	XP_016865452.1:p.Phe2354=
XM_017009964.2:c.7059T>C	XP_016865453.1:p.Phe2353=
XM_017009965.1:c.7059T>C	XP_016865454.1:p.Phe2353=
XM_017009966.2:c.6981T>C	XP_016865455.1:p.Phe2327=
XM_017009967.1:c.6966T>C	XP_016865456.1:p.Phe2322=
XM_017009968.2:c.7062T>C	XP_016865457.1:p.Phe2354=
XM_017009969.2:c.7062T>C	XP_016865458.1:p.Phe2354=
XM_017009970.2:c.7062T>C	XP_016865459.1:p.Phe2354=
XM_017009971.2:c.7062T>C	XP_016865460.1:p.Phe2354=
XM_017009972.1:c.180T>C	XP_016865461.1:p.Phe60=
XM_017009973.1:c.180T>C	XP_016865462.1:p.Phe60=
XM_017009974.2:c.7062T>C	XP_016865463.1:p.Phe2354=
NR_003149.2:n.7078T>C