Canonical Allele Identifier: CA1562882066

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745613C= , CM000667.2:g.90745613C=	GRCh38
NC_000005.9:g.90041430C= , CM000667.1:g.90041430C=	GRCh37
NC_000005.8:g.90077186C=	NCBI36
NG_007083.1:g.191814C=
NG_007083.2:g.221270C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10792C= MANE Select	ENSP00000384582.2:p.Pro3598=
ENST00000639431.1:c.265+69404C=	ENSP00000491057.1:n.265+69404C=
ENST00000640374.1:n.3936C=
ENST00000640464.1:n.1211C=
ENST00000405460.6:c.10792C=	ENSP00000384582.2:p.Pro3598=
ENST00000509621.1:c.3489C=
NM_032119.3:c.10792C=	NP_115495.3:p.Pro3598=
NR_003149.1:n.10805C=
XM_011543675.1:c.10789C=	XP_011541977.1:p.Pro3597=
XM_011543676.1:c.10711C=	XP_011541978.1:p.Pro3571=
XM_011543677.1:c.8095C=	XP_011541979.1:p.Pro2699=
XM_011543678.1:c.10792C=	XP_011541980.1:p.Pro3598=
XM_011543679.1:c.*14C=	XP_011541981.1:n.*14C=
NM_032119.4:c.10792C= MANE Select	NP_115495.3:p.Pro3598=
XM_017009963.2:c.10813C=	XP_016865452.1:p.Pro3605=
XM_017009964.2:c.10810C=	XP_016865453.1:p.Pro3604=
XM_017009965.1:c.10810C=	XP_016865454.1:p.Pro3604=
XM_017009966.2:c.10732C=	XP_016865455.1:p.Pro3578=
XM_017009967.1:c.10717C=	XP_016865456.1:p.Pro3573=
XM_017009968.2:c.10813C=	XP_016865457.1:p.Pro3605=
XM_017009969.2:c.10813C=	XP_016865458.1:p.Pro3605=
XM_017009970.2:c.10813C=	XP_016865459.1:p.Pro3605=
XM_017009971.2:c.10813C=	XP_016865460.1:p.Pro3605=
XM_017009972.1:c.3931C=	XP_016865461.1:p.Pro1311=
XM_017009973.1:c.3910C=	XP_016865462.1:p.Pro1304=
XM_017009974.2:c.*14C=	XP_016865463.1:n.*14C=
NR_003149.2:n.10808C=