Canonical Allele Identifier: CA445404549

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988550T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692733T>C , CM000667.2:g.90692733T>C	GRCh38
NC_000005.9:g.89988550T>C , CM000667.1:g.89988550T>C	GRCh37
NC_000005.8:g.90024306T>C	NCBI36
NG_007083.1:g.138934T>C
NG_007083.2:g.168390T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7080T>C MANE Select	ENSP00000384582.2:p.Arg2360=
ENST00000639431.1:c.265+16524T>C	ENSP00000491057.1:n.265+16524T>C
ENST00000639473.1:n.2539T>C
ENST00000640012.1:c.887T>C
ENST00000640374.1:n.224T>C
ENST00000640403.1:c.4371T>C	ENSP00000492531.1:p.Arg1457=
ENST00000640779.1:c.1809T>C
ENST00000405460.6:c.7080T>C	ENSP00000384582.2:p.Arg2360=
NM_032119.3:c.7080T>C	NP_115495.3:p.Arg2360=
NR_003149.1:n.7093T>C
XM_011543675.1:c.7077T>C	XP_011541977.1:p.Arg2359=
XM_011543676.1:c.6999T>C	XP_011541978.1:p.Arg2333=
XM_011543677.1:c.4383T>C	XP_011541979.1:p.Arg1461=
XM_011543678.1:c.7080T>C	XP_011541980.1:p.Arg2360=
XM_011543679.1:c.7080T>C	XP_011541981.1:p.Arg2360=
NM_032119.4:c.7080T>C MANE Select	NP_115495.3:p.Arg2360=
XM_017009963.2:c.7080T>C	XP_016865452.1:p.Arg2360=
XM_017009964.2:c.7077T>C	XP_016865453.1:p.Arg2359=
XM_017009965.1:c.7077T>C	XP_016865454.1:p.Arg2359=
XM_017009966.2:c.6999T>C	XP_016865455.1:p.Arg2333=
XM_017009967.1:c.6984T>C	XP_016865456.1:p.Arg2328=
XM_017009968.2:c.7080T>C	XP_016865457.1:p.Arg2360=
XM_017009969.2:c.7080T>C	XP_016865458.1:p.Arg2360=
XM_017009970.2:c.7080T>C	XP_016865459.1:p.Arg2360=
XM_017009971.2:c.7080T>C	XP_016865460.1:p.Arg2360=
XM_017009972.1:c.198T>C	XP_016865461.1:p.Arg66=
XM_017009973.1:c.198T>C	XP_016865462.1:p.Arg66=
XM_017009974.2:c.7080T>C	XP_016865463.1:p.Arg2360=
NR_003149.2:n.7096T>C