Canonical Allele Identifier: CA445468252

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90106815A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810998A>C , CM000667.2:g.90810998A>C	GRCh38
NC_000005.9:g.90106815A>C , CM000667.1:g.90106815A>C	GRCh37
NC_000005.8:g.90142571A>C	NCBI36
NG_007083.1:g.257199A>C
NG_007083.2:g.286655A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15738A>C MANE Select	ENSP00000384582.2:p.Arg5246=
ENST00000425867.3:c.4692A>C	ENSP00000392618.3:p.Arg1564=
ENST00000638510.1:n.3005A>C
ENST00000639431.1:c.265+134789A>C	ENSP00000491057.1:n.265+134789A>C
ENST00000640407.1:c.2148A>C	ENSP00000491425.1:p.Arg716=
ENST00000405460.6:c.15738A>C	ENSP00000384582.2:p.Arg5246=
ENST00000425867.2:c.2721A>C	ENSP00000392618.2:p.Arg907=
NM_032119.3:c.15738A>C	NP_115495.3:p.Arg5246=
NR_003149.1:n.15751A>C
XM_011543675.1:c.15735A>C	XP_011541977.1:p.Arg5245=
XM_011543676.1:c.15657A>C	XP_011541978.1:p.Arg5219=
XM_011543677.1:c.13041A>C	XP_011541979.1:p.Arg4347=
NM_032119.4:c.15738A>C MANE Select	NP_115495.3:p.Arg5246=
XM_017009963.2:c.15759A>C	XP_016865452.1:p.Arg5253=
XM_017009964.2:c.15756A>C	XP_016865453.1:p.Arg5252=
XM_017009965.1:c.15756A>C	XP_016865454.1:p.Arg5252=
XM_017009966.2:c.15678A>C	XP_016865455.1:p.Arg5226=
XM_017009967.1:c.15663A>C	XP_016865456.1:p.Arg5221=
XM_017009968.2:c.15579A>C	XP_016865457.1:p.Arg5193=
XM_017009969.2:c.15759A>C	XP_016865458.1:p.Arg5253=
XM_017009972.1:c.8877A>C	XP_016865461.1:p.Arg2959=
XM_017009973.1:c.8856A>C	XP_016865462.1:p.Arg2952=
NR_003149.2:n.15754A>C