Canonical Allele Identifier: CA2767420620

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692886_90692887insAC , CM000667.2:g.90692886_90692887insAC	GRCh38
NC_000005.9:g.89988703_89988704insAC , CM000667.1:g.89988703_89988704insAC	GRCh37
NC_000005.8:g.90024459_90024460insAC	NCBI36
NG_007083.1:g.139087_139088insAC
NG_007083.2:g.168543_168544insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7133+100_7133+101insAC MANE Select	ENSP00000384582.2:n.7133+100_7133+101insAC
ENST00000639431.1:c.265+16677_265+16678insAC	ENSP00000491057.1:n.265+16677_265+16678insAC
ENST00000639473.1:n.2592+100_2592+101insAC
ENST00000640012.1:c.940+100_940+101insAC
ENST00000640374.1:n.277+100_277+101insAC
ENST00000640403.1:c.4424+100_4424+101insAC	ENSP00000492531.1:n.4424+100_4424+101insAC
ENST00000640779.1:c.1862+100_1862+101insAC
ENST00000405460.6:c.7133+100_7133+101insAC	ENSP00000384582.2:n.7133+100_7133+101insAC
NM_032119.3:c.7133+100_7133+101insAC	NP_115495.3:n.7133+100_7133+101insAC
NR_003149.1:n.7146+100_7146+101insAC
XM_011543675.1:c.7130+100_7130+101insAC	XP_011541977.1:n.7130+100_7130+101insAC
XM_011543676.1:c.7052+100_7052+101insAC	XP_011541978.1:n.7052+100_7052+101insAC
XM_011543677.1:c.4436+100_4436+101insAC	XP_011541979.1:n.4436+100_4436+101insAC
XM_011543678.1:c.7133+100_7133+101insAC	XP_011541980.1:n.7133+100_7133+101insAC
XM_011543679.1:c.7133+100_7133+101insAC	XP_011541981.1:n.7133+100_7133+101insAC
NM_032119.4:c.7133+100_7133+101insAC MANE Select	NP_115495.3:n.7133+100_7133+101insAC
XM_017009963.2:c.7133+100_7133+101insAC	XP_016865452.1:n.7133+100_7133+101insAC
XM_017009964.2:c.7130+100_7130+101insAC	XP_016865453.1:n.7130+100_7130+101insAC
XM_017009965.1:c.7130+100_7130+101insAC	XP_016865454.1:n.7130+100_7130+101insAC
XM_017009966.2:c.7052+100_7052+101insAC	XP_016865455.1:n.7052+100_7052+101insAC
XM_017009967.1:c.7037+100_7037+101insAC	XP_016865456.1:n.7037+100_7037+101insAC
XM_017009968.2:c.7133+100_7133+101insAC	XP_016865457.1:n.7133+100_7133+101insAC
XM_017009969.2:c.7133+100_7133+101insAC	XP_016865458.1:n.7133+100_7133+101insAC
XM_017009970.2:c.7133+100_7133+101insAC	XP_016865459.1:n.7133+100_7133+101insAC
XM_017009971.2:c.7133+100_7133+101insAC	XP_016865460.1:n.7133+100_7133+101insAC
XM_017009972.1:c.251+100_251+101insAC	XP_016865461.1:n.251+100_251+101insAC
XM_017009973.1:c.251+100_251+101insAC	XP_016865462.1:n.251+100_251+101insAC
XM_017009974.2:c.7133+100_7133+101insAC	XP_016865463.1:n.7133+100_7133+101insAC
NR_003149.2:n.7149+100_7149+101insAC