Canonical Allele Identifier: CA360377085

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059131G>A (hg19) ; chr5:g.90763314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763314G>A , CM000667.2:g.90763314G>A	GRCh38
NC_000005.9:g.90059131G>A , CM000667.1:g.90059131G>A	GRCh37
NC_000005.8:g.90094887G>A	NCBI36
NG_007083.1:g.209515G>A
NG_007083.2:g.238971G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12130G>A MANE Select	ENSP00000384582.2:p.Asp4044Asn
ENST00000425867.3:c.1084G>A	ENSP00000392618.3:p.Asp362Asn
ENST00000639431.1:c.265+87105G>A	ENSP00000491057.1:n.265+87105G>A
ENST00000640464.1:n.2549G>A
ENST00000640729.1:n.707G>A
ENST00000405460.6:c.12130G>A	ENSP00000384582.2:p.Asp4044Asn
NM_032119.3:c.12130G>A	NP_115495.3:p.Asp4044Asn
NR_003149.1:n.12143G>A
XM_011543675.1:c.12127G>A	XP_011541977.1:p.Asp4043Asn
XM_011543676.1:c.12049G>A	XP_011541978.1:p.Asp4017Asn
XM_011543677.1:c.9433G>A	XP_011541979.1:p.Asp3145Asn
XM_011543678.1:c.12130G>A	XP_011541980.1:p.Asp4044Asn
NM_032119.4:c.12130G>A MANE Select	NP_115495.3:p.Asp4044Asn
XM_017009963.2:c.12151G>A	XP_016865452.1:p.Asp4051Asn
XM_017009964.2:c.12148G>A	XP_016865453.1:p.Asp4050Asn
XM_017009965.1:c.12148G>A	XP_016865454.1:p.Asp4050Asn
XM_017009966.2:c.12070G>A	XP_016865455.1:p.Asp4024Asn
XM_017009967.1:c.12055G>A	XP_016865456.1:p.Asp4019Asn
XM_017009968.2:c.12151G>A	XP_016865457.1:p.Asp4051Asn
XM_017009969.2:c.12151G>A	XP_016865458.1:p.Asp4051Asn
XM_017009970.2:c.12151G>A	XP_016865459.1:p.Asp4051Asn
XM_017009971.2:c.12151G>A	XP_016865460.1:p.Asp4051Asn
XM_017009972.1:c.5269G>A	XP_016865461.1:p.Asp1757Asn
XM_017009973.1:c.5248G>A	XP_016865462.1:p.Asp1750Asn
NR_003149.2:n.12146G>A