Canonical Allele Identifier: CA1562859262

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692644A= , CM000667.2:g.90692644A=	GRCh38
NC_000005.9:g.89988461A= , CM000667.1:g.89988461A=	GRCh37
NC_000005.8:g.90024217A=	NCBI36
NG_007083.1:g.138845A=
NG_007083.2:g.168301A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6991A= MANE Select	ENSP00000384582.2:p.Thr2331=
ENST00000639431.1:c.265+16435A=	ENSP00000491057.1:n.265+16435A=
ENST00000639473.1:n.2450A=
ENST00000640012.1:c.798A=
ENST00000640374.1:n.135A=
ENST00000640403.1:c.4282A=	ENSP00000492531.1:p.Thr1428=
ENST00000640779.1:c.1720A=
ENST00000405460.6:c.6991A=	ENSP00000384582.2:p.Thr2331=
NM_032119.3:c.6991A=	NP_115495.3:p.Thr2331=
NR_003149.1:n.7004A=
XM_011543675.1:c.6988A=	XP_011541977.1:p.Thr2330=
XM_011543676.1:c.6910A=	XP_011541978.1:p.Thr2304=
XM_011543677.1:c.4294A=	XP_011541979.1:p.Thr1432=
XM_011543678.1:c.6991A=	XP_011541980.1:p.Thr2331=
XM_011543679.1:c.6991A=	XP_011541981.1:p.Thr2331=
NM_032119.4:c.6991A= MANE Select	NP_115495.3:p.Thr2331=
XM_017009963.2:c.6991A=	XP_016865452.1:p.Thr2331=
XM_017009964.2:c.6988A=	XP_016865453.1:p.Thr2330=
XM_017009965.1:c.6988A=	XP_016865454.1:p.Thr2330=
XM_017009966.2:c.6910A=	XP_016865455.1:p.Thr2304=
XM_017009967.1:c.6895A=	XP_016865456.1:p.Thr2299=
XM_017009968.2:c.6991A=	XP_016865457.1:p.Thr2331=
XM_017009969.2:c.6991A=	XP_016865458.1:p.Thr2331=
XM_017009970.2:c.6991A=	XP_016865459.1:p.Thr2331=
XM_017009971.2:c.6991A=	XP_016865460.1:p.Thr2331=
XM_017009972.1:c.109A=	XP_016865461.1:p.Thr37=
XM_017009973.1:c.109A=	XP_016865462.1:p.Thr37=
XM_017009974.2:c.6991A=	XP_016865463.1:p.Thr2331=
NR_003149.2:n.7007A=