Canonical Allele Identifier: CA1562902286

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791208A= , CM000667.2:g.90791208A=	GRCh38
NC_000005.9:g.90087025A= , CM000667.1:g.90087025A=	GRCh37
NC_000005.8:g.90122781A=	NCBI36
NG_007083.1:g.237409A=
NG_007083.2:g.266865A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14379A= MANE Select	ENSP00000384582.2:p.Thr4793=
ENST00000425867.3:c.3333A=	ENSP00000392618.3:p.Thr1111=
ENST00000507314.2:c.54A=	ENSP00000491299.1:p.Thr18=
ENST00000638510.1:n.1646A=
ENST00000638585.1:n.145A=
ENST00000638975.1:c.1008A=	ENSP00000492630.1:p.Thr336=
ENST00000639431.1:c.265+114999A=	ENSP00000491057.1:n.265+114999A=
ENST00000640407.1:c.789A=	ENSP00000491425.1:p.Thr263=
ENST00000405460.6:c.14379A=	ENSP00000384582.2:p.Thr4793=
ENST00000425867.2:c.1362A=	ENSP00000392618.2:p.Thr454=
ENST00000507314.1:n.54A=
NM_032119.3:c.14379A=	NP_115495.3:p.Thr4793=
NR_003149.1:n.14392A=
XM_011543675.1:c.14376A=	XP_011541977.1:p.Thr4792=
XM_011543676.1:c.14298A=	XP_011541978.1:p.Thr4766=
XM_011543677.1:c.11682A=	XP_011541979.1:p.Thr3894=
XM_011543678.1:c.14379A=	XP_011541980.1:p.Thr4793=
NM_032119.4:c.14379A= MANE Select	NP_115495.3:p.Thr4793=
XM_017009963.2:c.14400A=	XP_016865452.1:p.Thr4800=
XM_017009964.2:c.14397A=	XP_016865453.1:p.Thr4799=
XM_017009965.1:c.14397A=	XP_016865454.1:p.Thr4799=
XM_017009966.2:c.14319A=	XP_016865455.1:p.Thr4773=
XM_017009967.1:c.14304A=	XP_016865456.1:p.Thr4768=
XM_017009968.2:c.14400A=	XP_016865457.1:p.Thr4800=
XM_017009969.2:c.14400A=	XP_016865458.1:p.Thr4800=
XM_017009970.2:c.14400A=	XP_016865459.1:p.Thr4800=
XM_017009971.2:c.14400A=	XP_016865460.1:p.Thr4800=
XM_017009972.1:c.7518A=	XP_016865461.1:p.Thr2506=
XM_017009973.1:c.7497A=	XP_016865462.1:p.Thr2499=
NR_003149.2:n.14395A=