Canonical Allele Identifier: CA1562956749

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90914002T= , CM000667.2:g.90914002T=	GRCh38
NC_000005.9:g.90209819T= , CM000667.1:g.90209819T=	GRCh37
NC_000005.8:g.90245575T=	NCBI36
NG_007083.1:g.360203T=
NG_007083.2:g.389659T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17856+50145T= MANE Select	ENSP00000384582.2:n.17856+50145T=
ENST00000425867.3:c.6810+50145T=	ENSP00000392618.3:n.6810+50145T=
ENST00000638510.1:n.5123+50145T=
ENST00000638990.1:c.1068+50145T=
ENST00000639431.1:c.266-71342T=	ENSP00000491057.1:n.266-71342T=
ENST00000640407.1:c.4305+50145T=	ENSP00000491425.1:n.4305+50145T=
ENST00000640815.1:c.-61+14679T=	ENSP00000491767.1:n.-61+14679T=
ENST00000405460.6:c.17856+50145T=	ENSP00000384582.2:n.17856+50145T=
ENST00000425867.2:c.4839+50145T=	ENSP00000392618.2:n.4839+50145T=
NM_032119.3:c.17856+50145T=	NP_115495.3:n.17856+50145T=
NR_003149.1:n.17869+50145T=
XM_011543675.1:c.17853+50145T=	XP_011541977.1:n.17853+50145T=
XM_011543676.1:c.17775+50145T=	XP_011541978.1:n.17775+50145T=
XM_011543677.1:c.15159+50145T=	XP_011541979.1:n.15159+50145T=
NM_032119.4:c.17856+50145T= MANE Select	NP_115495.3:n.17856+50145T=
XM_017009963.2:c.17877+50145T=	XP_016865452.1:n.17877+50145T=
XM_017009964.2:c.17874+50145T=	XP_016865453.1:n.17874+50145T=
XM_017009965.1:c.17874+50145T=	XP_016865454.1:n.17874+50145T=
XM_017009966.2:c.17796+50145T=	XP_016865455.1:n.17796+50145T=
XM_017009967.1:c.17781+50145T=	XP_016865456.1:n.17781+50145T=
XM_017009968.2:c.17697+50145T=	XP_016865457.1:n.17697+50145T=
XM_017009969.2:c.17877+50145T=	XP_016865458.1:n.17877+50145T=
XM_017009972.1:c.10995+50145T=	XP_016865461.1:n.10995+50145T=
XM_017009973.1:c.10974+50145T=	XP_016865462.1:n.10974+50145T=
NR_003149.2:n.17872+50145T=