Canonical Allele Identifier: CA360396165

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712311-A-T
• MyVariant Identifiers: chr5:g.90008128A>T (hg19) ; chr5:g.90712311A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712311A>T , CM000667.2:g.90712311A>T	GRCh38
NC_000005.9:g.90008128A>T , CM000667.1:g.90008128A>T	GRCh37
NC_000005.8:g.90043884A>T	NCBI36
NG_007083.1:g.158512A>T
NG_007083.2:g.187968A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9067A>T MANE Select	ENSP00000384582.2:p.Arg3023Trp
ENST00000639431.1:c.265+36102A>T	ENSP00000491057.1:n.265+36102A>T
ENST00000639473.1:n.4526A>T
ENST00000640012.1:c.2874A>T
ENST00000640374.1:n.2211A>T
ENST00000640779.1:c.3796A>T
ENST00000405460.6:c.9067A>T	ENSP00000384582.2:p.Arg3023Trp
ENST00000509621.1:c.1764A>T
NM_032119.3:c.9067A>T	NP_115495.3:p.Arg3023Trp
NR_003149.1:n.9080A>T
XM_011543675.1:c.9064A>T	XP_011541977.1:p.Arg3022Trp
XM_011543676.1:c.8986A>T	XP_011541978.1:p.Arg2996Trp
XM_011543677.1:c.6370A>T	XP_011541979.1:p.Arg2124Trp
XM_011543678.1:c.9067A>T	XP_011541980.1:p.Arg3023Trp
XM_011543679.1:c.9067A>T	XP_011541981.1:p.Arg3023Trp
NM_032119.4:c.9067A>T MANE Select	NP_115495.3:p.Arg3023Trp
XM_017009963.2:c.9088A>T	XP_016865452.1:p.Arg3030Trp
XM_017009964.2:c.9085A>T	XP_016865453.1:p.Arg3029Trp
XM_017009965.1:c.9085A>T	XP_016865454.1:p.Arg3029Trp
XM_017009966.2:c.9007A>T	XP_016865455.1:p.Arg3003Trp
XM_017009967.1:c.8992A>T	XP_016865456.1:p.Arg2998Trp
XM_017009968.2:c.9088A>T	XP_016865457.1:p.Arg3030Trp
XM_017009969.2:c.9088A>T	XP_016865458.1:p.Arg3030Trp
XM_017009970.2:c.9088A>T	XP_016865459.1:p.Arg3030Trp
XM_017009971.2:c.9088A>T	XP_016865460.1:p.Arg3030Trp
XM_017009972.1:c.2206A>T	XP_016865461.1:p.Arg736Trp
XM_017009973.1:c.2185A>T	XP_016865462.1:p.Arg729Trp
XM_017009974.2:c.9088A>T	XP_016865463.1:p.Arg3030Trp
NR_003149.2:n.9083A>T