Canonical Allele Identifier: CA917526149

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1561539178

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692982_90692983insT , CM000667.2:g.90692982_90692983insT	GRCh38
NC_000005.9:g.89988799_89988800insT , CM000667.1:g.89988799_89988800insT	GRCh37
NC_000005.8:g.90024555_90024556insT	NCBI36
NG_007083.1:g.139183_139184insT
NG_007083.2:g.168639_168640insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+196_7133+197insT MANE Select	ENSP00000384582.2:n.7133+196_7133+197insT
ENST00000639431.1:c.265+16773_265+16774insT	ENSP00000491057.1:n.265+16773_265+16774insT
ENST00000639473.1:n.2592+196_2592+197insT
ENST00000640012.1:c.940+196_940+197insT
ENST00000640374.1:n.277+196_277+197insT
ENST00000640403.1:c.4424+196_4424+197insT	ENSP00000492531.1:n.4424+196_4424+197insT
ENST00000640779.1:c.1862+196_1862+197insT
ENST00000405460.6:c.7133+196_7133+197insT	ENSP00000384582.2:n.7133+196_7133+197insT
NM_032119.3:c.7133+196_7133+197insT	NP_115495.3:n.7133+196_7133+197insT
NR_003149.1:n.7146+196_7146+197insT
XM_011543675.1:c.7130+196_7130+197insT	XP_011541977.1:n.7130+196_7130+197insT
XM_011543676.1:c.7052+196_7052+197insT	XP_011541978.1:n.7052+196_7052+197insT
XM_011543677.1:c.4436+196_4436+197insT	XP_011541979.1:n.4436+196_4436+197insT
XM_011543678.1:c.7133+196_7133+197insT	XP_011541980.1:n.7133+196_7133+197insT
XM_011543679.1:c.7133+196_7133+197insT	XP_011541981.1:n.7133+196_7133+197insT
NM_032119.4:c.7133+196_7133+197insT MANE Select	NP_115495.3:n.7133+196_7133+197insT
XM_017009963.2:c.7133+196_7133+197insT	XP_016865452.1:n.7133+196_7133+197insT
XM_017009964.2:c.7130+196_7130+197insT	XP_016865453.1:n.7130+196_7130+197insT
XM_017009965.1:c.7130+196_7130+197insT	XP_016865454.1:n.7130+196_7130+197insT
XM_017009966.2:c.7052+196_7052+197insT	XP_016865455.1:n.7052+196_7052+197insT
XM_017009967.1:c.7037+196_7037+197insT	XP_016865456.1:n.7037+196_7037+197insT
XM_017009968.2:c.7133+196_7133+197insT	XP_016865457.1:n.7133+196_7133+197insT
XM_017009969.2:c.7133+196_7133+197insT	XP_016865458.1:n.7133+196_7133+197insT
XM_017009970.2:c.7133+196_7133+197insT	XP_016865459.1:n.7133+196_7133+197insT
XM_017009971.2:c.7133+196_7133+197insT	XP_016865460.1:n.7133+196_7133+197insT
XM_017009972.1:c.251+196_251+197insT	XP_016865461.1:n.251+196_251+197insT
XM_017009973.1:c.251+196_251+197insT	XP_016865462.1:n.251+196_251+197insT
XM_017009974.2:c.7133+196_7133+197insT	XP_016865463.1:n.7133+196_7133+197insT
NR_003149.2:n.7149+196_7149+197insT