Canonical Allele Identifier: CA1562885447

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90753705C= , CM000667.2:g.90753705C=	GRCh38
NC_000005.9:g.90049522C= , CM000667.1:g.90049522C=	GRCh37
NC_000005.8:g.90085278C=	NCBI36
NG_007083.1:g.199906C=
NG_007083.2:g.229362C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11253C= MANE Select	ENSP00000384582.2:p.Tyr3751=
ENST00000425867.3:c.384C=	ENSP00000392618.3:p.Tyr128=
ENST00000639431.1:c.265+77496C=	ENSP00000491057.1:n.265+77496C=
ENST00000640374.1:n.4397C=
ENST00000640464.1:n.1672C=
ENST00000405460.6:c.11253C=	ENSP00000384582.2:p.Tyr3751=
ENST00000509621.1:c.3950C=
NM_032119.3:c.11253C=	NP_115495.3:p.Tyr3751=
NR_003149.1:n.11266C=
XM_011543675.1:c.11250C=	XP_011541977.1:p.Tyr3750=
XM_011543676.1:c.11172C=	XP_011541978.1:p.Tyr3724=
XM_011543677.1:c.8556C=	XP_011541979.1:p.Tyr2852=
XM_011543678.1:c.11253C=	XP_011541980.1:p.Tyr3751=
NM_032119.4:c.11253C= MANE Select	NP_115495.3:p.Tyr3751=
XM_017009963.2:c.11274C=	XP_016865452.1:p.Tyr3758=
XM_017009964.2:c.11271C=	XP_016865453.1:p.Tyr3757=
XM_017009965.1:c.11271C=	XP_016865454.1:p.Tyr3757=
XM_017009966.2:c.11193C=	XP_016865455.1:p.Tyr3731=
XM_017009967.1:c.11178C=	XP_016865456.1:p.Tyr3726=
XM_017009968.2:c.11274C=	XP_016865457.1:p.Tyr3758=
XM_017009969.2:c.11274C=	XP_016865458.1:p.Tyr3758=
XM_017009970.2:c.11274C=	XP_016865459.1:p.Tyr3758=
XM_017009971.2:c.11274C=	XP_016865460.1:p.Tyr3758=
XM_017009972.1:c.4392C=	XP_016865461.1:p.Tyr1464=
XM_017009973.1:c.4371C=	XP_016865462.1:p.Tyr1457=
NR_003149.2:n.11269C=