Canonical Allele Identifier: CA1562901705

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789833C= , CM000667.2:g.90789833C=	GRCh38
NC_000005.9:g.90085650C= , CM000667.1:g.90085650C=	GRCh37
NC_000005.8:g.90121406C=	NCBI36
NG_007083.1:g.236034C=
NG_007083.2:g.265490C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14025C= MANE Select	ENSP00000384582.2:p.Gly4675=
ENST00000425867.3:c.2979C=	ENSP00000392618.3:p.Gly993=
ENST00000638510.1:n.1292C=
ENST00000638975.1:c.654C=	ENSP00000492630.1:p.Gly218=
ENST00000639431.1:c.265+113624C=	ENSP00000491057.1:n.265+113624C=
ENST00000640407.1:c.435C=	ENSP00000491425.1:p.Gly145=
ENST00000405460.6:c.14025C=	ENSP00000384582.2:p.Gly4675=
ENST00000425867.2:c.1008C=	ENSP00000392618.2:p.Gly336=
NM_032119.3:c.14025C=	NP_115495.3:p.Gly4675=
NR_003149.1:n.14038C=
XM_011543675.1:c.14022C=	XP_011541977.1:p.Gly4674=
XM_011543676.1:c.13944C=	XP_011541978.1:p.Gly4648=
XM_011543677.1:c.11328C=	XP_011541979.1:p.Gly3776=
XM_011543678.1:c.14025C=	XP_011541980.1:p.Gly4675=
NM_032119.4:c.14025C= MANE Select	NP_115495.3:p.Gly4675=
XM_017009963.2:c.14046C=	XP_016865452.1:p.Gly4682=
XM_017009964.2:c.14043C=	XP_016865453.1:p.Gly4681=
XM_017009965.1:c.14043C=	XP_016865454.1:p.Gly4681=
XM_017009966.2:c.13965C=	XP_016865455.1:p.Gly4655=
XM_017009967.1:c.13950C=	XP_016865456.1:p.Gly4650=
XM_017009968.2:c.14046C=	XP_016865457.1:p.Gly4682=
XM_017009969.2:c.14046C=	XP_016865458.1:p.Gly4682=
XM_017009970.2:c.14046C=	XP_016865459.1:p.Gly4682=
XM_017009971.2:c.14046C=	XP_016865460.1:p.Gly4682=
XM_017009972.1:c.7164C=	XP_016865461.1:p.Gly2388=
XM_017009973.1:c.7143C=	XP_016865462.1:p.Gly2381=
NR_003149.2:n.14041C=