Canonical Allele Identifier: CA1562889864

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763305G= , CM000667.2:g.90763305G=	GRCh38
NC_000005.9:g.90059122G= , CM000667.1:g.90059122G=	GRCh37
NC_000005.8:g.90094878G=	NCBI36
NG_007083.1:g.209506G=
NG_007083.2:g.238962G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12121G= MANE Select	ENSP00000384582.2:p.Val4041=
ENST00000425867.3:c.1075G=	ENSP00000392618.3:p.Val359=
ENST00000639431.1:c.265+87096G=	ENSP00000491057.1:n.265+87096G=
ENST00000640464.1:n.2540G=
ENST00000640729.1:n.698G=
ENST00000405460.6:c.12121G=	ENSP00000384582.2:p.Val4041=
NM_032119.3:c.12121G=	NP_115495.3:p.Val4041=
NR_003149.1:n.12134G=
XM_011543675.1:c.12118G=	XP_011541977.1:p.Val4040=
XM_011543676.1:c.12040G=	XP_011541978.1:p.Val4014=
XM_011543677.1:c.9424G=	XP_011541979.1:p.Val3142=
XM_011543678.1:c.12121G=	XP_011541980.1:p.Val4041=
NM_032119.4:c.12121G= MANE Select	NP_115495.3:p.Val4041=
XM_017009963.2:c.12142G=	XP_016865452.1:p.Val4048=
XM_017009964.2:c.12139G=	XP_016865453.1:p.Val4047=
XM_017009965.1:c.12139G=	XP_016865454.1:p.Val4047=
XM_017009966.2:c.12061G=	XP_016865455.1:p.Val4021=
XM_017009967.1:c.12046G=	XP_016865456.1:p.Val4016=
XM_017009968.2:c.12142G=	XP_016865457.1:p.Val4048=
XM_017009969.2:c.12142G=	XP_016865458.1:p.Val4048=
XM_017009970.2:c.12142G=	XP_016865459.1:p.Val4048=
XM_017009971.2:c.12142G=	XP_016865460.1:p.Val4048=
XM_017009972.1:c.5260G=	XP_016865461.1:p.Val1754=
XM_017009973.1:c.5239G=	XP_016865462.1:p.Val1747=
NR_003149.2:n.12137G=