Canonical Allele Identifier: CA1562889879

Gene: ADGRV1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12166G= MANE Select	ENSP00000384582.2:p.Val4056=
ENST00000425867.3:c.1120G=	ENSP00000392618.3:p.Val374=
ENST00000639431.1:c.265+87141G=	ENSP00000491057.1:n.265+87141G=
ENST00000640464.1:n.2585G=
ENST00000640729.1:n.743G=
ENST00000405460.6:c.12166G=	ENSP00000384582.2:p.Val4056=
NM_032119.3:c.12166G=	NP_115495.3:p.Val4056=
NR_003149.1:n.12179G=
XM_011543675.1:c.12163G=	XP_011541977.1:p.Val4055=
XM_011543676.1:c.12085G=	XP_011541978.1:p.Val4029=
XM_011543677.1:c.9469G=	XP_011541979.1:p.Val3157=
XM_011543678.1:c.12166G=	XP_011541980.1:p.Val4056=
NM_032119.4:c.12166G= MANE Select	NP_115495.3:p.Val4056=
XM_017009963.2:c.12187G=	XP_016865452.1:p.Val4063=
XM_017009964.2:c.12184G=	XP_016865453.1:p.Val4062=
XM_017009965.1:c.12184G=	XP_016865454.1:p.Val4062=
XM_017009966.2:c.12106G=	XP_016865455.1:p.Val4036=
XM_017009967.1:c.12091G=	XP_016865456.1:p.Val4031=
XM_017009968.2:c.12187G=	XP_016865457.1:p.Val4063=
XM_017009969.2:c.12187G=	XP_016865458.1:p.Val4063=
XM_017009970.2:c.12187G=	XP_016865459.1:p.Val4063=
XM_017009971.2:c.12187G=	XP_016865460.1:p.Val4063=
XM_017009972.1:c.5305G=	XP_016865461.1:p.Val1769=
XM_017009973.1:c.5284G=	XP_016865462.1:p.Val1762=
NR_003149.2:n.12182G=