Canonical Allele Identifier: CA1562980222

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965491A= , CM000667.2:g.90965491A=	GRCh38
NC_000005.9:g.90261308A= , CM000667.1:g.90261308A=	GRCh37
NC_000005.8:g.90297064A=	NCBI36
NG_007083.1:g.411692A=
NG_007083.2:g.441148A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17933A= MANE Select	ENSP00000384582.2:p.His5978=
ENST00000425867.3:c.6887A=	ENSP00000392618.3:p.His2296=
ENST00000638510.1:n.5200A=
ENST00000638990.1:c.1145A=
ENST00000639431.1:c.266-19853A=	ENSP00000491057.1:n.266-19853A=
ENST00000639707.1:c.17A=	ENSP00000492328.1:p.His6=
ENST00000639821.1:c.17A=	ENSP00000492216.1:p.His6=
ENST00000640369.1:c.17A=	ENSP00000491401.1:p.His6=
ENST00000640407.1:c.4382A=	ENSP00000491425.1:n.4382A=
ENST00000640815.1:c.17A=	ENSP00000491767.1:p.His6=
ENST00000405460.6:c.17933A=	ENSP00000384582.2:p.His5978=
ENST00000425867.2:c.4916A=	ENSP00000392618.2:p.His1639=
NM_032119.3:c.17933A=	NP_115495.3:p.His5978=
NR_003149.1:n.17946A=
XM_011543675.1:c.17930A=	XP_011541977.1:p.His5977=
XM_011543676.1:c.17852A=	XP_011541978.1:p.His5951=
XM_011543677.1:c.15236A=	XP_011541979.1:p.His5079=
NM_032119.4:c.17933A= MANE Select	NP_115495.3:p.His5978=
XM_017009963.2:c.17954A=	XP_016865452.1:p.His5985=
XM_017009964.2:c.17951A=	XP_016865453.1:p.His5984=
XM_017009965.1:c.17951A=	XP_016865454.1:p.His5984=
XM_017009966.2:c.17873A=	XP_016865455.1:p.His5958=
XM_017009967.1:c.17858A=	XP_016865456.1:p.His5953=
XM_017009968.2:c.17774A=	XP_016865457.1:p.His5925=
XM_017009969.2:c.17954A=	XP_016865458.1:p.His5985=
XM_017009972.1:c.11072A=	XP_016865461.1:p.His3691=
XM_017009973.1:c.11051A=	XP_016865462.1:p.His3684=
NR_003149.2:n.17949A=