Canonical Allele Identifier: CA1562990543

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90985501A= , CM000667.2:g.90985501A=	GRCh38
NC_000005.9:g.90281318A= , CM000667.1:g.90281318A=	GRCh37
NC_000005.8:g.90317074A=	NCBI36
NG_007083.1:g.431702A=
NG_007083.2:g.461158A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18131A= MANE Select	NP_115495.3:p.Tyr6044=
ENST00000405460.9:c.18131A= MANE Select	ENSP00000384582.2:p.Tyr6044=
NM_032119.3:c.18131A=	NP_115495.3:p.Tyr6044=
NR_003149.1:n.18144A=
NR_003149.2:n.18147A=
ENST00000405460.6:c.18131A=	ENSP00000384582.2:p.Tyr6044=
ENST00000425867.2:c.5114A=	ENSP00000392618.2:p.Tyr1705=
ENST00000425867.3:c.7085A=	ENSP00000392618.3:p.Tyr2362=
ENST00000638510.1:n.5398A=
ENST00000638990.1:c.1343A=
ENST00000639431.1:c.423A=	ENSP00000491057.1:n.423A=
ENST00000639707.1:c.215A=	ENSP00000492328.1:p.Tyr72=
ENST00000639821.1:c.215A=	ENSP00000492216.1:p.Tyr72=
ENST00000640369.1:c.215A=	ENSP00000491401.1:p.Tyr72=
ENST00000640407.1:c.4580A=	ENSP00000491425.1:n.4580A=
ENST00000640815.1:c.215A=	ENSP00000491767.1:p.Tyr72=
XM_011543675.1:c.18128A=	XP_011541977.1:p.Tyr6043=
XM_011543676.1:c.18050A=	XP_011541978.1:p.Tyr6017=
XM_011543677.1:c.15434A=	XP_011541979.1:p.Tyr5145=
XM_017009963.2:c.18152A=	XP_016865452.1:p.Tyr6051=
XM_017009964.2:c.18149A=	XP_016865453.1:p.Tyr6050=
XM_017009965.1:c.18149A=	XP_016865454.1:p.Tyr6050=
XM_017009966.2:c.18071A=	XP_016865455.1:p.Tyr6024=
XM_017009967.1:c.18056A=	XP_016865456.1:p.Tyr6019=
XM_017009968.2:c.17972A=	XP_016865457.1:p.Tyr5991=
XM_017009969.2:c.18152A=	XP_016865458.1:p.Tyr6051=
XM_017009972.1:c.11270A=	XP_016865461.1:p.Tyr3757=
XM_017009973.1:c.11249A=	XP_016865462.1:p.Tyr3750=