Canonical Allele Identifier: CA360401305

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086930G>C (hg19) ; chr5:g.90791113G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791113G>C , CM000667.2:g.90791113G>C	GRCh38
NC_000005.9:g.90086930G>C , CM000667.1:g.90086930G>C	GRCh37
NC_000005.8:g.90122686G>C	NCBI36
NG_007083.1:g.237314G>C
NG_007083.2:g.266770G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14284G>C MANE Select	ENSP00000384582.2:p.Gly4762Arg
ENST00000425867.3:c.3238G>C	ENSP00000392618.3:p.Gly1080Arg
ENST00000638510.1:n.1551G>C
ENST00000638585.1:n.50G>C
ENST00000638975.1:c.913G>C	ENSP00000492630.1:p.Gly305Arg
ENST00000639431.1:c.265+114904G>C	ENSP00000491057.1:n.265+114904G>C
ENST00000640407.1:c.694G>C	ENSP00000491425.1:p.Gly232Arg
ENST00000405460.6:c.14284G>C	ENSP00000384582.2:p.Gly4762Arg
ENST00000425867.2:c.1267G>C	ENSP00000392618.2:p.Gly423Arg
NM_032119.3:c.14284G>C	NP_115495.3:p.Gly4762Arg
NR_003149.1:n.14297G>C
XM_011543675.1:c.14281G>C	XP_011541977.1:p.Gly4761Arg
XM_011543676.1:c.14203G>C	XP_011541978.1:p.Gly4735Arg
XM_011543677.1:c.11587G>C	XP_011541979.1:p.Gly3863Arg
XM_011543678.1:c.14284G>C	XP_011541980.1:p.Gly4762Arg
NM_032119.4:c.14284G>C MANE Select	NP_115495.3:p.Gly4762Arg
XM_017009963.2:c.14305G>C	XP_016865452.1:p.Gly4769Arg
XM_017009964.2:c.14302G>C	XP_016865453.1:p.Gly4768Arg
XM_017009965.1:c.14302G>C	XP_016865454.1:p.Gly4768Arg
XM_017009966.2:c.14224G>C	XP_016865455.1:p.Gly4742Arg
XM_017009967.1:c.14209G>C	XP_016865456.1:p.Gly4737Arg
XM_017009968.2:c.14305G>C	XP_016865457.1:p.Gly4769Arg
XM_017009969.2:c.14305G>C	XP_016865458.1:p.Gly4769Arg
XM_017009970.2:c.14305G>C	XP_016865459.1:p.Gly4769Arg
XM_017009971.2:c.14305G>C	XP_016865460.1:p.Gly4769Arg
XM_017009972.1:c.7423G>C	XP_016865461.1:p.Gly2475Arg
XM_017009973.1:c.7402G>C	XP_016865462.1:p.Gly2468Arg
NR_003149.2:n.14300G>C