Canonical Allele Identifier: CA1562980167

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965395G= , CM000667.2:g.90965395G=	GRCh38
NC_000005.9:g.90261212G= , CM000667.1:g.90261212G=	GRCh37
NC_000005.8:g.90296968G=	NCBI36
NG_007083.1:g.411596G=
NG_007083.2:g.441052G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17857-20G= MANE Select	ENSP00000384582.2:n.17857-20G=
ENST00000425867.3:c.6811-20G=	ENSP00000392618.3:n.6811-20G=
ENST00000638510.1:n.5124-20G=
ENST00000638990.1:c.1069-20G=
ENST00000639431.1:c.266-19949G=	ENSP00000491057.1:n.266-19949G=
ENST00000639707.1:c.-60-20G=	ENSP00000492328.1:n.-60-20G=
ENST00000639821.1:c.-60-20G=	ENSP00000492216.1:n.-60-20G=
ENST00000640369.1:c.-60-20G=	ENSP00000491401.1:n.-60-20G=
ENST00000640407.1:c.4306-20G=	ENSP00000491425.1:n.4306-20G=
ENST00000640815.1:c.-60-20G=	ENSP00000491767.1:n.-60-20G=
ENST00000405460.6:c.17857-20G=	ENSP00000384582.2:n.17857-20G=
ENST00000425867.2:c.4840-20G=	ENSP00000392618.2:n.4840-20G=
NM_032119.3:c.17857-20G=	NP_115495.3:n.17857-20G=
NR_003149.1:n.17870-20G=
XM_011543675.1:c.17854-20G=	XP_011541977.1:n.17854-20G=
XM_011543676.1:c.17776-20G=	XP_011541978.1:n.17776-20G=
XM_011543677.1:c.15160-20G=	XP_011541979.1:n.15160-20G=
NM_032119.4:c.17857-20G= MANE Select	NP_115495.3:n.17857-20G=
XM_017009963.2:c.17878-20G=	XP_016865452.1:n.17878-20G=
XM_017009964.2:c.17875-20G=	XP_016865453.1:n.17875-20G=
XM_017009965.1:c.17875-20G=	XP_016865454.1:n.17875-20G=
XM_017009966.2:c.17797-20G=	XP_016865455.1:n.17797-20G=
XM_017009967.1:c.17782-20G=	XP_016865456.1:n.17782-20G=
XM_017009968.2:c.17698-20G=	XP_016865457.1:n.17698-20G=
XM_017009969.2:c.17878-20G=	XP_016865458.1:n.17878-20G=
XM_017009972.1:c.10996-20G=	XP_016865461.1:n.10996-20G=
XM_017009973.1:c.10975-20G=	XP_016865462.1:n.10975-20G=
NR_003149.2:n.17873-20G=