Canonical Allele Identifier: CA1562980225

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965496C= , CM000667.2:g.90965496C=	GRCh38
NC_000005.9:g.90261313C= , CM000667.1:g.90261313C=	GRCh37
NC_000005.8:g.90297069C=	NCBI36
NG_007083.1:g.411697C=
NG_007083.2:g.441153C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17938C= MANE Select	ENSP00000384582.2:p.Leu5980=
ENST00000425867.3:c.6892C=	ENSP00000392618.3:p.Leu2298=
ENST00000638510.1:n.5205C=
ENST00000638990.1:c.1150C=
ENST00000639431.1:c.266-19848C=	ENSP00000491057.1:n.266-19848C=
ENST00000639707.1:c.22C=	ENSP00000492328.1:p.Leu8=
ENST00000639821.1:c.22C=	ENSP00000492216.1:p.Leu8=
ENST00000640369.1:c.22C=	ENSP00000491401.1:p.Leu8=
ENST00000640407.1:c.4387C=	ENSP00000491425.1:n.4387C=
ENST00000640815.1:c.22C=	ENSP00000491767.1:p.Leu8=
ENST00000405460.6:c.17938C=	ENSP00000384582.2:p.Leu5980=
ENST00000425867.2:c.4921C=	ENSP00000392618.2:p.Leu1641=
NM_032119.3:c.17938C=	NP_115495.3:p.Leu5980=
NR_003149.1:n.17951C=
XM_011543675.1:c.17935C=	XP_011541977.1:p.Leu5979=
XM_011543676.1:c.17857C=	XP_011541978.1:p.Leu5953=
XM_011543677.1:c.15241C=	XP_011541979.1:p.Leu5081=
NM_032119.4:c.17938C= MANE Select	NP_115495.3:p.Leu5980=
XM_017009963.2:c.17959C=	XP_016865452.1:p.Leu5987=
XM_017009964.2:c.17956C=	XP_016865453.1:p.Leu5986=
XM_017009965.1:c.17956C=	XP_016865454.1:p.Leu5986=
XM_017009966.2:c.17878C=	XP_016865455.1:p.Leu5960=
XM_017009967.1:c.17863C=	XP_016865456.1:p.Leu5955=
XM_017009968.2:c.17779C=	XP_016865457.1:p.Leu5927=
XM_017009969.2:c.17959C=	XP_016865458.1:p.Leu5987=
XM_017009972.1:c.11077C=	XP_016865461.1:p.Leu3693=
XM_017009973.1:c.11056C=	XP_016865462.1:p.Leu3686=
NR_003149.2:n.17954C=