Canonical Allele Identifier: CA1562882099

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745692A= , CM000667.2:g.90745692A=	GRCh38
NC_000005.9:g.90041509A= , CM000667.1:g.90041509A=	GRCh37
NC_000005.8:g.90077265A=	NCBI36
NG_007083.1:g.191893A=
NG_007083.2:g.221349A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10871A= MANE Select	ENSP00000384582.2:p.Gln3624=
ENST00000425867.3:c.2A=	ENSP00000392618.3:p.Gln1=
ENST00000639431.1:c.265+69483A=	ENSP00000491057.1:n.265+69483A=
ENST00000640374.1:n.4015A=
ENST00000640464.1:n.1290A=
ENST00000405460.6:c.10871A=	ENSP00000384582.2:p.Gln3624=
ENST00000509621.1:c.3568A=
NM_032119.3:c.10871A=	NP_115495.3:p.Gln3624=
NR_003149.1:n.10884A=
XM_011543675.1:c.10868A=	XP_011541977.1:p.Gln3623=
XM_011543676.1:c.10790A=	XP_011541978.1:p.Gln3597=
XM_011543677.1:c.8174A=	XP_011541979.1:p.Gln2725=
XM_011543678.1:c.10871A=	XP_011541980.1:p.Gln3624=
NM_032119.4:c.10871A= MANE Select	NP_115495.3:p.Gln3624=
XM_017009963.2:c.10892A=	XP_016865452.1:p.Gln3631=
XM_017009964.2:c.10889A=	XP_016865453.1:p.Gln3630=
XM_017009965.1:c.10889A=	XP_016865454.1:p.Gln3630=
XM_017009966.2:c.10811A=	XP_016865455.1:p.Gln3604=
XM_017009967.1:c.10796A=	XP_016865456.1:p.Gln3599=
XM_017009968.2:c.10892A=	XP_016865457.1:p.Gln3631=
XM_017009969.2:c.10892A=	XP_016865458.1:p.Gln3631=
XM_017009970.2:c.10892A=	XP_016865459.1:p.Gln3631=
XM_017009971.2:c.10892A=	XP_016865460.1:p.Gln3631=
XM_017009972.1:c.4010A=	XP_016865461.1:p.Gln1337=
XM_017009973.1:c.3989A=	XP_016865462.1:p.Gln1330=
NR_003149.2:n.10887A=