Canonical Allele Identifier: CA445467503

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086914A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791097A>C , CM000667.2:g.90791097A>C	GRCh38
NC_000005.9:g.90086914A>C , CM000667.1:g.90086914A>C	GRCh37
NC_000005.8:g.90122670A>C	NCBI36
NG_007083.1:g.237298A>C
NG_007083.2:g.266754A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14268A>C MANE Select	ENSP00000384582.2:p.Ala4756=
ENST00000425867.3:c.3222A>C	ENSP00000392618.3:p.Ala1074=
ENST00000638510.1:n.1535A>C
ENST00000638585.1:n.34A>C
ENST00000638975.1:c.897A>C	ENSP00000492630.1:p.Ala299=
ENST00000639431.1:c.265+114888A>C	ENSP00000491057.1:n.265+114888A>C
ENST00000640407.1:c.678A>C	ENSP00000491425.1:p.Ala226=
ENST00000405460.6:c.14268A>C	ENSP00000384582.2:p.Ala4756=
ENST00000425867.2:c.1251A>C	ENSP00000392618.2:p.Ala417=
NM_032119.3:c.14268A>C	NP_115495.3:p.Ala4756=
NR_003149.1:n.14281A>C
XM_011543675.1:c.14265A>C	XP_011541977.1:p.Ala4755=
XM_011543676.1:c.14187A>C	XP_011541978.1:p.Ala4729=
XM_011543677.1:c.11571A>C	XP_011541979.1:p.Ala3857=
XM_011543678.1:c.14268A>C	XP_011541980.1:p.Ala4756=
NM_032119.4:c.14268A>C MANE Select	NP_115495.3:p.Ala4756=
XM_017009963.2:c.14289A>C	XP_016865452.1:p.Ala4763=
XM_017009964.2:c.14286A>C	XP_016865453.1:p.Ala4762=
XM_017009965.1:c.14286A>C	XP_016865454.1:p.Ala4762=
XM_017009966.2:c.14208A>C	XP_016865455.1:p.Ala4736=
XM_017009967.1:c.14193A>C	XP_016865456.1:p.Ala4731=
XM_017009968.2:c.14289A>C	XP_016865457.1:p.Ala4763=
XM_017009969.2:c.14289A>C	XP_016865458.1:p.Ala4763=
XM_017009970.2:c.14289A>C	XP_016865459.1:p.Ala4763=
XM_017009971.2:c.14289A>C	XP_016865460.1:p.Ala4763=
XM_017009972.1:c.7407A>C	XP_016865461.1:p.Ala2469=
XM_017009973.1:c.7386A>C	XP_016865462.1:p.Ala2462=
NR_003149.2:n.14284A>C