Canonical Allele Identifier: CA1562911581

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810898A= , CM000667.2:g.90810898A=	GRCh38
NC_000005.9:g.90106715A= , CM000667.1:g.90106715A=	GRCh37
NC_000005.8:g.90142471A=	NCBI36
NG_007083.1:g.257099A=
NG_007083.2:g.286555A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15638A= MANE Select	ENSP00000384582.2:p.Asn5213=
ENST00000425867.3:c.4592A=	ENSP00000392618.3:p.Asn1531=
ENST00000638510.1:n.2905A=
ENST00000639431.1:c.265+134689A=	ENSP00000491057.1:n.265+134689A=
ENST00000640407.1:c.2048A=	ENSP00000491425.1:p.Asn683=
ENST00000405460.6:c.15638A=	ENSP00000384582.2:p.Asn5213=
ENST00000425867.2:c.2621A=	ENSP00000392618.2:p.Asn874=
NM_032119.3:c.15638A=	NP_115495.3:p.Asn5213=
NR_003149.1:n.15651A=
XM_011543675.1:c.15635A=	XP_011541977.1:p.Asn5212=
XM_011543676.1:c.15557A=	XP_011541978.1:p.Asn5186=
XM_011543677.1:c.12941A=	XP_011541979.1:p.Asn4314=
NM_032119.4:c.15638A= MANE Select	NP_115495.3:p.Asn5213=
XM_017009963.2:c.15659A=	XP_016865452.1:p.Asn5220=
XM_017009964.2:c.15656A=	XP_016865453.1:p.Asn5219=
XM_017009965.1:c.15656A=	XP_016865454.1:p.Asn5219=
XM_017009966.2:c.15578A=	XP_016865455.1:p.Asn5193=
XM_017009967.1:c.15563A=	XP_016865456.1:p.Asn5188=
XM_017009968.2:c.15479A=	XP_016865457.1:p.Asn5160=
XM_017009969.2:c.15659A=	XP_016865458.1:p.Asn5220=
XM_017009972.1:c.8777A=	XP_016865461.1:p.Asn2926=
XM_017009973.1:c.8756A=	XP_016865462.1:p.Asn2919=
NR_003149.2:n.15654A=