Canonical Allele Identifier: CA360372100

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988597G>C (hg19) ; chr5:g.90692780G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692780G>C , CM000667.2:g.90692780G>C	GRCh38
NC_000005.9:g.89988597G>C , CM000667.1:g.89988597G>C	GRCh37
NC_000005.8:g.90024353G>C	NCBI36
NG_007083.1:g.138981G>C
NG_007083.2:g.168437G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7127G>C MANE Select	ENSP00000384582.2:p.Arg2376Thr
ENST00000639431.1:c.265+16571G>C	ENSP00000491057.1:n.265+16571G>C
ENST00000639473.1:n.2586G>C
ENST00000640012.1:c.934G>C
ENST00000640374.1:n.271G>C
ENST00000640403.1:c.4418G>C	ENSP00000492531.1:p.Arg1473Thr
ENST00000640779.1:c.1856G>C
ENST00000405460.6:c.7127G>C	ENSP00000384582.2:p.Arg2376Thr
NM_032119.3:c.7127G>C	NP_115495.3:p.Arg2376Thr
NR_003149.1:n.7140G>C
XM_011543675.1:c.7124G>C	XP_011541977.1:p.Arg2375Thr
XM_011543676.1:c.7046G>C	XP_011541978.1:p.Arg2349Thr
XM_011543677.1:c.4430G>C	XP_011541979.1:p.Arg1477Thr
XM_011543678.1:c.7127G>C	XP_011541980.1:p.Arg2376Thr
XM_011543679.1:c.7127G>C	XP_011541981.1:p.Arg2376Thr
NM_032119.4:c.7127G>C MANE Select	NP_115495.3:p.Arg2376Thr
XM_017009963.2:c.7127G>C	XP_016865452.1:p.Arg2376Thr
XM_017009964.2:c.7124G>C	XP_016865453.1:p.Arg2375Thr
XM_017009965.1:c.7124G>C	XP_016865454.1:p.Arg2375Thr
XM_017009966.2:c.7046G>C	XP_016865455.1:p.Arg2349Thr
XM_017009967.1:c.7031G>C	XP_016865456.1:p.Arg2344Thr
XM_017009968.2:c.7127G>C	XP_016865457.1:p.Arg2376Thr
XM_017009969.2:c.7127G>C	XP_016865458.1:p.Arg2376Thr
XM_017009970.2:c.7127G>C	XP_016865459.1:p.Arg2376Thr
XM_017009971.2:c.7127G>C	XP_016865460.1:p.Arg2376Thr
XM_017009972.1:c.245G>C	XP_016865461.1:p.Arg82Thr
XM_017009973.1:c.245G>C	XP_016865462.1:p.Arg82Thr
XM_017009974.2:c.7127G>C	XP_016865463.1:p.Arg2376Thr
NR_003149.2:n.7143G>C