Canonical Allele Identifier: CA360377102

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90763315-A-T
• MyVariant Identifiers: chr5:g.90059132A>T (hg19) ; chr5:g.90763315A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763315A>T , CM000667.2:g.90763315A>T	GRCh38
NC_000005.9:g.90059132A>T , CM000667.1:g.90059132A>T	GRCh37
NC_000005.8:g.90094888A>T	NCBI36
NG_007083.1:g.209516A>T
NG_007083.2:g.238972A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12131A>T MANE Select	ENSP00000384582.2:p.Asp4044Val
ENST00000425867.3:c.1085A>T	ENSP00000392618.3:p.Asp362Val
ENST00000639431.1:c.265+87106A>T	ENSP00000491057.1:n.265+87106A>T
ENST00000640464.1:n.2550A>T
ENST00000640729.1:n.708A>T
ENST00000405460.6:c.12131A>T	ENSP00000384582.2:p.Asp4044Val
NM_032119.3:c.12131A>T	NP_115495.3:p.Asp4044Val
NR_003149.1:n.12144A>T
XM_011543675.1:c.12128A>T	XP_011541977.1:p.Asp4043Val
XM_011543676.1:c.12050A>T	XP_011541978.1:p.Asp4017Val
XM_011543677.1:c.9434A>T	XP_011541979.1:p.Asp3145Val
XM_011543678.1:c.12131A>T	XP_011541980.1:p.Asp4044Val
NM_032119.4:c.12131A>T MANE Select	NP_115495.3:p.Asp4044Val
XM_017009963.2:c.12152A>T	XP_016865452.1:p.Asp4051Val
XM_017009964.2:c.12149A>T	XP_016865453.1:p.Asp4050Val
XM_017009965.1:c.12149A>T	XP_016865454.1:p.Asp4050Val
XM_017009966.2:c.12071A>T	XP_016865455.1:p.Asp4024Val
XM_017009967.1:c.12056A>T	XP_016865456.1:p.Asp4019Val
XM_017009968.2:c.12152A>T	XP_016865457.1:p.Asp4051Val
XM_017009969.2:c.12152A>T	XP_016865458.1:p.Asp4051Val
XM_017009970.2:c.12152A>T	XP_016865459.1:p.Asp4051Val
XM_017009971.2:c.12152A>T	XP_016865460.1:p.Asp4051Val
XM_017009972.1:c.5270A>T	XP_016865461.1:p.Asp1757Val
XM_017009973.1:c.5249A>T	XP_016865462.1:p.Asp1750Val
NR_003149.2:n.12147A>T