Canonical Allele Identifier: CA1562918287

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823521G= , CM000667.2:g.90823521G=	GRCh38
NC_000005.9:g.90119338G= , CM000667.1:g.90119338G=	GRCh37
NC_000005.8:g.90155094G=	NCBI36
NG_007083.1:g.269722G=
NG_007083.2:g.299178G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16293G= MANE Select	ENSP00000384582.2:p.Gln5431=
ENST00000425867.3:c.5247G=	ENSP00000392618.3:p.Gln1749=
ENST00000638510.1:n.3560G=
ENST00000639431.1:c.265+147312G=	ENSP00000491057.1:n.265+147312G=
ENST00000640061.1:n.128+1339G=
ENST00000640407.1:c.2703G=	ENSP00000491425.1:p.Gln901=
ENST00000405460.6:c.16293G=	ENSP00000384582.2:p.Gln5431=
ENST00000425867.2:c.3276G=	ENSP00000392618.2:p.Gln1092=
NM_032119.3:c.16293G=	NP_115495.3:p.Gln5431=
NR_003149.1:n.16306G=
XM_011543675.1:c.16290G=	XP_011541977.1:p.Gln5430=
XM_011543676.1:c.16212G=	XP_011541978.1:p.Gln5404=
XM_011543677.1:c.13596G=	XP_011541979.1:p.Gln4532=
NM_032119.4:c.16293G= MANE Select	NP_115495.3:p.Gln5431=
XM_017009963.2:c.16314G=	XP_016865452.1:p.Gln5438=
XM_017009964.2:c.16311G=	XP_016865453.1:p.Gln5437=
XM_017009965.1:c.16311G=	XP_016865454.1:p.Gln5437=
XM_017009966.2:c.16233G=	XP_016865455.1:p.Gln5411=
XM_017009967.1:c.16218G=	XP_016865456.1:p.Gln5406=
XM_017009968.2:c.16134G=	XP_016865457.1:p.Gln5378=
XM_017009969.2:c.16314G=	XP_016865458.1:p.Gln5438=
XM_017009972.1:c.9432G=	XP_016865461.1:p.Gln3144=
XM_017009973.1:c.9411G=	XP_016865462.1:p.Gln3137=
NR_003149.2:n.16309G=