Canonical Allele Identifier: CA1563051738

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91128366T= , CM000667.2:g.91128366T=	GRCh38
NC_000005.9:g.90424183T= , CM000667.1:g.90424183T=	GRCh37
NC_000005.8:g.90459939T=	NCBI36
NG_007083.1:g.574567T=
NG_007083.2:g.604023T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.18433-21664T= MANE Select	ENSP00000384582.2:n.18433-21664T=
ENST00000425867.3:c.7387-21664T=	ENSP00000392618.3:n.7387-21664T=
ENST00000638510.1:n.5700-21664T=
ENST00000638990.1:c.1645-21664T=
ENST00000639212.1:n.353-21664T=
ENST00000639530.1:n.301-21664T=
ENST00000639821.1:c.516+26026T=	ENSP00000492216.1:n.516+26026T=
ENST00000640256.1:n.301-24855T=
ENST00000640407.1:c.4882-21664T=	ENSP00000491425.1:n.4882-21664T=
ENST00000640815.1:c.517-21664T=	ENSP00000491767.1:n.517-21664T=
ENST00000405460.6:c.18433-21664T=	ENSP00000384582.2:n.18433-21664T=
ENST00000425867.2:c.5416-21664T=	ENSP00000392618.2:n.5416-21664T=
NM_032119.3:c.18433-21664T=	NP_115495.3:n.18433-21664T=
NR_003149.1:n.18446-21664T=
XM_011543675.1:c.18430-21664T=	XP_011541977.1:n.18430-21664T=
XM_011543676.1:c.18352-21664T=	XP_011541978.1:n.18352-21664T=
XM_011543677.1:c.15736-21664T=	XP_011541979.1:n.15736-21664T=
NM_032119.4:c.18433-21664T= MANE Select	NP_115495.3:n.18433-21664T=
XM_017009963.2:c.18454-21664T=	XP_016865452.1:n.18454-21664T=
XM_017009964.2:c.18451-21664T=	XP_016865453.1:n.18451-21664T=
XM_017009965.1:c.18451-21664T=	XP_016865454.1:n.18451-21664T=
XM_017009966.2:c.18373-21664T=	XP_016865455.1:n.18373-21664T=
XM_017009967.1:c.18358-21664T=	XP_016865456.1:n.18358-21664T=
XM_017009968.2:c.18274-21664T=	XP_016865457.1:n.18274-21664T=
XM_017009969.2:c.18453+26026T=	XP_016865458.1:n.18453+26026T=
XM_017009972.1:c.11572-21664T=	XP_016865461.1:n.11572-21664T=
XM_017009973.1:c.11551-21664T=	XP_016865462.1:n.11551-21664T=
NR_003149.2:n.18449-21664T=