Canonical Allele Identifier: CA360377487

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1756719636
• MyVariant Identifiers: chr5:g.90059167G>A (hg19) ; chr5:g.90763350G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763350G>A , CM000667.2:g.90763350G>A	GRCh38
NC_000005.9:g.90059167G>A , CM000667.1:g.90059167G>A	GRCh37
NC_000005.8:g.90094923G>A	NCBI36
NG_007083.1:g.209551G>A
NG_007083.2:g.239007G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12166G>A MANE Select	ENSP00000384582.2:p.Val4056Met
ENST00000425867.3:c.1120G>A	ENSP00000392618.3:p.Val374Met
ENST00000639431.1:c.265+87141G>A	ENSP00000491057.1:n.265+87141G>A
ENST00000640464.1:n.2585G>A
ENST00000640729.1:n.743G>A
ENST00000405460.6:c.12166G>A	ENSP00000384582.2:p.Val4056Met
NM_032119.3:c.12166G>A	NP_115495.3:p.Val4056Met
NR_003149.1:n.12179G>A
XM_011543675.1:c.12163G>A	XP_011541977.1:p.Val4055Met
XM_011543676.1:c.12085G>A	XP_011541978.1:p.Val4029Met
XM_011543677.1:c.9469G>A	XP_011541979.1:p.Val3157Met
XM_011543678.1:c.12166G>A	XP_011541980.1:p.Val4056Met
NM_032119.4:c.12166G>A MANE Select	NP_115495.3:p.Val4056Met
XM_017009963.2:c.12187G>A	XP_016865452.1:p.Val4063Met
XM_017009964.2:c.12184G>A	XP_016865453.1:p.Val4062Met
XM_017009965.1:c.12184G>A	XP_016865454.1:p.Val4062Met
XM_017009966.2:c.12106G>A	XP_016865455.1:p.Val4036Met
XM_017009967.1:c.12091G>A	XP_016865456.1:p.Val4031Met
XM_017009968.2:c.12187G>A	XP_016865457.1:p.Val4063Met
XM_017009969.2:c.12187G>A	XP_016865458.1:p.Val4063Met
XM_017009970.2:c.12187G>A	XP_016865459.1:p.Val4063Met
XM_017009971.2:c.12187G>A	XP_016865460.1:p.Val4063Met
XM_017009972.1:c.5305G>A	XP_016865461.1:p.Val1769Met
XM_017009973.1:c.5284G>A	XP_016865462.1:p.Val1762Met
NR_003149.2:n.12182G>A