Canonical Allele Identifier: CA1562859284

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692694T= , CM000667.2:g.90692694T=	GRCh38
NC_000005.9:g.89988511T= , CM000667.1:g.89988511T=	GRCh37
NC_000005.8:g.90024267T=	NCBI36
NG_007083.1:g.138895T=
NG_007083.2:g.168351T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7041T= MANE Select	ENSP00000384582.2:p.Asp2347=
ENST00000639431.1:c.265+16485T=	ENSP00000491057.1:n.265+16485T=
ENST00000639473.1:n.2500T=
ENST00000640012.1:c.848T=
ENST00000640374.1:n.185T=
ENST00000640403.1:c.4332T=	ENSP00000492531.1:p.Asp1444=
ENST00000640779.1:c.1770T=
ENST00000405460.6:c.7041T=	ENSP00000384582.2:p.Asp2347=
NM_032119.3:c.7041T=	NP_115495.3:p.Asp2347=
NR_003149.1:n.7054T=
XM_011543675.1:c.7038T=	XP_011541977.1:p.Asp2346=
XM_011543676.1:c.6960T=	XP_011541978.1:p.Asp2320=
XM_011543677.1:c.4344T=	XP_011541979.1:p.Asp1448=
XM_011543678.1:c.7041T=	XP_011541980.1:p.Asp2347=
XM_011543679.1:c.7041T=	XP_011541981.1:p.Asp2347=
NM_032119.4:c.7041T= MANE Select	NP_115495.3:p.Asp2347=
XM_017009963.2:c.7041T=	XP_016865452.1:p.Asp2347=
XM_017009964.2:c.7038T=	XP_016865453.1:p.Asp2346=
XM_017009965.1:c.7038T=	XP_016865454.1:p.Asp2346=
XM_017009966.2:c.6960T=	XP_016865455.1:p.Asp2320=
XM_017009967.1:c.6945T=	XP_016865456.1:p.Asp2315=
XM_017009968.2:c.7041T=	XP_016865457.1:p.Asp2347=
XM_017009969.2:c.7041T=	XP_016865458.1:p.Asp2347=
XM_017009970.2:c.7041T=	XP_016865459.1:p.Asp2347=
XM_017009971.2:c.7041T=	XP_016865460.1:p.Asp2347=
XM_017009972.1:c.159T=	XP_016865461.1:p.Asp53=
XM_017009973.1:c.159T=	XP_016865462.1:p.Asp53=
XM_017009974.2:c.7041T=	XP_016865463.1:p.Asp2347=
NR_003149.2:n.7057T=