Canonical Allele Identifier: CA1562886186

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755051T= , CM000667.2:g.90755051T=	GRCh38
NC_000005.9:g.90050868T= , CM000667.1:g.90050868T=	GRCh37
NC_000005.8:g.90086624T=	NCBI36
NG_007083.1:g.201252T=
NG_007083.2:g.230708T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11446T= MANE Select	ENSP00000384582.2:p.Leu3816=
ENST00000425867.3:c.577T=	ENSP00000392618.3:p.Leu193=
ENST00000639431.1:c.265+78842T=	ENSP00000491057.1:n.265+78842T=
ENST00000640374.1:n.4590T=
ENST00000640464.1:n.1865T=
ENST00000405460.6:c.11446T=	ENSP00000384582.2:p.Leu3816=
ENST00000509621.1:c.4143T=
NM_032119.3:c.11446T=	NP_115495.3:p.Leu3816=
NR_003149.1:n.11459T=
XM_011543675.1:c.11443T=	XP_011541977.1:p.Leu3815=
XM_011543676.1:c.11365T=	XP_011541978.1:p.Leu3789=
XM_011543677.1:c.8749T=	XP_011541979.1:p.Leu2917=
XM_011543678.1:c.11446T=	XP_011541980.1:p.Leu3816=
NM_032119.4:c.11446T= MANE Select	NP_115495.3:p.Leu3816=
XM_017009963.2:c.11467T=	XP_016865452.1:p.Leu3823=
XM_017009964.2:c.11464T=	XP_016865453.1:p.Leu3822=
XM_017009965.1:c.11464T=	XP_016865454.1:p.Leu3822=
XM_017009966.2:c.11386T=	XP_016865455.1:p.Leu3796=
XM_017009967.1:c.11371T=	XP_016865456.1:p.Leu3791=
XM_017009968.2:c.11467T=	XP_016865457.1:p.Leu3823=
XM_017009969.2:c.11467T=	XP_016865458.1:p.Leu3823=
XM_017009970.2:c.11467T=	XP_016865459.1:p.Leu3823=
XM_017009971.2:c.11467T=	XP_016865460.1:p.Leu3823=
XM_017009972.1:c.4585T=	XP_016865461.1:p.Leu1529=
XM_017009973.1:c.4564T=	XP_016865462.1:p.Leu1522=
NR_003149.2:n.11462T=