Canonical Allele Identifier: CA360406717

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90103541G>C (hg19) ; chr5:g.90807724G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90807724G>C , CM000667.2:g.90807724G>C	GRCh38
NC_000005.9:g.90103541G>C , CM000667.1:g.90103541G>C	GRCh37
NC_000005.8:g.90139297G>C	NCBI36
NG_007083.1:g.253925G>C
NG_007083.2:g.283381G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14959G>C MANE Select	ENSP00000384582.2:p.Gly4987Arg
ENST00000425867.3:c.3913G>C	ENSP00000392618.3:p.Gly1305Arg
ENST00000638510.1:n.2226G>C
ENST00000638585.1:n.428-2509G>C
ENST00000639431.1:c.265+131515G>C	ENSP00000491057.1:n.265+131515G>C
ENST00000640407.1:c.1369G>C	ENSP00000491425.1:p.Gly457Arg
ENST00000405460.6:c.14959G>C	ENSP00000384582.2:p.Gly4987Arg
ENST00000425867.2:c.1942G>C	ENSP00000392618.2:p.Gly648Arg
NM_032119.3:c.14959G>C	NP_115495.3:p.Gly4987Arg
NR_003149.1:n.14972G>C
XM_011543675.1:c.14956G>C	XP_011541977.1:p.Gly4986Arg
XM_011543676.1:c.14878G>C	XP_011541978.1:p.Gly4960Arg
XM_011543677.1:c.12262G>C	XP_011541979.1:p.Gly4088Arg
XM_011543678.1:c.14959G>C	XP_011541980.1:p.Gly4987Arg
NM_032119.4:c.14959G>C MANE Select	NP_115495.3:p.Gly4987Arg
XM_017009963.2:c.14980G>C	XP_016865452.1:p.Gly4994Arg
XM_017009964.2:c.14977G>C	XP_016865453.1:p.Gly4993Arg
XM_017009965.1:c.14977G>C	XP_016865454.1:p.Gly4993Arg
XM_017009966.2:c.14899G>C	XP_016865455.1:p.Gly4967Arg
XM_017009967.1:c.14884G>C	XP_016865456.1:p.Gly4962Arg
XM_017009968.2:c.14805G>C	XP_016865457.1:p.Ala4935=
XM_017009969.2:c.14980G>C	XP_016865458.1:p.Gly4994Arg
XM_017009970.2:c.14980G>C	XP_016865459.1:p.Gly4994Arg
XM_017009971.2:c.14805G>C	XP_016865460.1:p.Ala4935=
XM_017009972.1:c.8098G>C	XP_016865461.1:p.Gly2700Arg
XM_017009973.1:c.8077G>C	XP_016865462.1:p.Gly2693Arg
NR_003149.2:n.14975G>C