Canonical Allele Identifier: CA1562889873

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763338C= , CM000667.2:g.90763338C=	GRCh38
NC_000005.9:g.90059155C= , CM000667.1:g.90059155C=	GRCh37
NC_000005.8:g.90094911C=	NCBI36
NG_007083.1:g.209539C=
NG_007083.2:g.238995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12154C= MANE Select	ENSP00000384582.2:p.Pro4052=
ENST00000425867.3:c.1108C=	ENSP00000392618.3:p.Pro370=
ENST00000639431.1:c.265+87129C=	ENSP00000491057.1:n.265+87129C=
ENST00000640464.1:n.2573C=
ENST00000640729.1:n.731C=
ENST00000405460.6:c.12154C=	ENSP00000384582.2:p.Pro4052=
NM_032119.3:c.12154C=	NP_115495.3:p.Pro4052=
NR_003149.1:n.12167C=
XM_011543675.1:c.12151C=	XP_011541977.1:p.Pro4051=
XM_011543676.1:c.12073C=	XP_011541978.1:p.Pro4025=
XM_011543677.1:c.9457C=	XP_011541979.1:p.Pro3153=
XM_011543678.1:c.12154C=	XP_011541980.1:p.Pro4052=
NM_032119.4:c.12154C= MANE Select	NP_115495.3:p.Pro4052=
XM_017009963.2:c.12175C=	XP_016865452.1:p.Pro4059=
XM_017009964.2:c.12172C=	XP_016865453.1:p.Pro4058=
XM_017009965.1:c.12172C=	XP_016865454.1:p.Pro4058=
XM_017009966.2:c.12094C=	XP_016865455.1:p.Pro4032=
XM_017009967.1:c.12079C=	XP_016865456.1:p.Pro4027=
XM_017009968.2:c.12175C=	XP_016865457.1:p.Pro4059=
XM_017009969.2:c.12175C=	XP_016865458.1:p.Pro4059=
XM_017009970.2:c.12175C=	XP_016865459.1:p.Pro4059=
XM_017009971.2:c.12175C=	XP_016865460.1:p.Pro4059=
XM_017009972.1:c.5293C=	XP_016865461.1:p.Pro1765=
XM_017009973.1:c.5272C=	XP_016865462.1:p.Pro1758=
NR_003149.2:n.12170C=