Canonical Allele Identifier: CA3340850

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745753T>C , CM000667.2:g.90745753T>C	GRCh38
NC_000005.9:g.90041570T>C , CM000667.1:g.90041570T>C	GRCh37
NC_000005.8:g.90077326T>C	NCBI36
NG_007083.1:g.191954T>C
NG_007083.2:g.221410T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10932T>C MANE Select	NP_115495.3:p.Ile3644=
ENST00000405460.9:c.10932T>C MANE Select	ENSP00000384582.2:p.Ile3644=
NM_032119.3:c.10932T>C	NP_115495.3:p.Ile3644=
NR_003149.1:n.10945T>C
NR_003149.2:n.10948T>C
ENST00000405460.6:c.10932T>C	ENSP00000384582.2:p.Ile3644=
ENST00000425867.3:c.63T>C	ENSP00000392618.3:p.Ile21=
ENST00000509621.1:c.3629T>C
ENST00000639431.1:c.265+69544T>C	ENSP00000491057.1:n.265+69544T>C
ENST00000640374.1:n.4076T>C
ENST00000640464.1:n.1351T>C
XM_011543675.1:c.10929T>C	XP_011541977.1:p.Ile3643=
XM_011543676.1:c.10851T>C	XP_011541978.1:p.Ile3617=
XM_011543677.1:c.8235T>C	XP_011541979.1:p.Ile2745=
XM_011543678.1:c.10932T>C	XP_011541980.1:p.Ile3644=
XM_017009963.2:c.10953T>C	XP_016865452.1:p.Ile3651=
XM_017009964.2:c.10950T>C	XP_016865453.1:p.Ile3650=
XM_017009965.1:c.10950T>C	XP_016865454.1:p.Ile3650=
XM_017009966.2:c.10872T>C	XP_016865455.1:p.Ile3624=
XM_017009967.1:c.10857T>C	XP_016865456.1:p.Ile3619=
XM_017009968.2:c.10953T>C	XP_016865457.1:p.Ile3651=
XM_017009969.2:c.10953T>C	XP_016865458.1:p.Ile3651=
XM_017009970.2:c.10953T>C	XP_016865459.1:p.Ile3651=
XM_017009971.2:c.10953T>C	XP_016865460.1:p.Ile3651=
XM_017009972.1:c.4071T>C	XP_016865461.1:p.Ile1357=
XM_017009973.1:c.4050T>C	XP_016865462.1:p.Ile1350=