Canonical Allele Identifier: CA1562918237

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823427C= , CM000667.2:g.90823427C=	GRCh38
NC_000005.9:g.90119244C= , CM000667.1:g.90119244C=	GRCh37
NC_000005.8:g.90155000C=	NCBI36
NG_007083.1:g.269628C=
NG_007083.2:g.299084C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16199C= MANE Select	ENSP00000384582.2:p.Ala5400=
ENST00000425867.3:c.5153C=	ENSP00000392618.3:p.Ala1718=
ENST00000638510.1:n.3466C=
ENST00000639431.1:c.265+147218C=	ENSP00000491057.1:n.265+147218C=
ENST00000640061.1:n.128+1245C=
ENST00000640407.1:c.2609C=	ENSP00000491425.1:p.Ala870=
ENST00000405460.6:c.16199C=	ENSP00000384582.2:p.Ala5400=
ENST00000425867.2:c.3182C=	ENSP00000392618.2:p.Ala1061=
NM_032119.3:c.16199C=	NP_115495.3:p.Ala5400=
NR_003149.1:n.16212C=
XM_011543675.1:c.16196C=	XP_011541977.1:p.Ala5399=
XM_011543676.1:c.16118C=	XP_011541978.1:p.Ala5373=
XM_011543677.1:c.13502C=	XP_011541979.1:p.Ala4501=
NM_032119.4:c.16199C= MANE Select	NP_115495.3:p.Ala5400=
XM_017009963.2:c.16220C=	XP_016865452.1:p.Ala5407=
XM_017009964.2:c.16217C=	XP_016865453.1:p.Ala5406=
XM_017009965.1:c.16217C=	XP_016865454.1:p.Ala5406=
XM_017009966.2:c.16139C=	XP_016865455.1:p.Ala5380=
XM_017009967.1:c.16124C=	XP_016865456.1:p.Ala5375=
XM_017009968.2:c.16040C=	XP_016865457.1:p.Ala5347=
XM_017009969.2:c.16220C=	XP_016865458.1:p.Ala5407=
XM_017009972.1:c.9338C=	XP_016865461.1:p.Ala3113=
XM_017009973.1:c.9317C=	XP_016865462.1:p.Ala3106=
NR_003149.2:n.16215C=