Canonical Allele Identifier: CA360396167

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008129G>C (hg19) ; chr5:g.90712312G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712312G>C , CM000667.2:g.90712312G>C	GRCh38
NC_000005.9:g.90008129G>C , CM000667.1:g.90008129G>C	GRCh37
NC_000005.8:g.90043885G>C	NCBI36
NG_007083.1:g.158513G>C
NG_007083.2:g.187969G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9068G>C MANE Select	ENSP00000384582.2:p.Arg3023Thr
ENST00000639431.1:c.265+36103G>C	ENSP00000491057.1:n.265+36103G>C
ENST00000639473.1:n.4527G>C
ENST00000640012.1:c.2875G>C
ENST00000640374.1:n.2212G>C
ENST00000640779.1:c.3797G>C
ENST00000405460.6:c.9068G>C	ENSP00000384582.2:p.Arg3023Thr
ENST00000509621.1:c.1765G>C
NM_032119.3:c.9068G>C	NP_115495.3:p.Arg3023Thr
NR_003149.1:n.9081G>C
XM_011543675.1:c.9065G>C	XP_011541977.1:p.Arg3022Thr
XM_011543676.1:c.8987G>C	XP_011541978.1:p.Arg2996Thr
XM_011543677.1:c.6371G>C	XP_011541979.1:p.Arg2124Thr
XM_011543678.1:c.9068G>C	XP_011541980.1:p.Arg3023Thr
XM_011543679.1:c.9068G>C	XP_011541981.1:p.Arg3023Thr
NM_032119.4:c.9068G>C MANE Select	NP_115495.3:p.Arg3023Thr
XM_017009963.2:c.9089G>C	XP_016865452.1:p.Arg3030Thr
XM_017009964.2:c.9086G>C	XP_016865453.1:p.Arg3029Thr
XM_017009965.1:c.9086G>C	XP_016865454.1:p.Arg3029Thr
XM_017009966.2:c.9008G>C	XP_016865455.1:p.Arg3003Thr
XM_017009967.1:c.8993G>C	XP_016865456.1:p.Arg2998Thr
XM_017009968.2:c.9089G>C	XP_016865457.1:p.Arg3030Thr
XM_017009969.2:c.9089G>C	XP_016865458.1:p.Arg3030Thr
XM_017009970.2:c.9089G>C	XP_016865459.1:p.Arg3030Thr
XM_017009971.2:c.9089G>C	XP_016865460.1:p.Arg3030Thr
XM_017009972.1:c.2207G>C	XP_016865461.1:p.Arg736Thr
XM_017009973.1:c.2186G>C	XP_016865462.1:p.Arg729Thr
XM_017009974.2:c.9089G>C	XP_016865463.1:p.Arg3030Thr
NR_003149.2:n.9084G>C