Canonical Allele Identifier: CA560899251

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1405213379
• gnomAD v2: 5-89999392-G-T
• gnomAD v3: 5-90703575-G-T
• gnomAD v4: 5-90703575-G-T
• MyVariant Identifiers: chr5:g.89999392G>T (hg19) ; chr5:g.90703575G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703575G>T , CM000667.2:g.90703575G>T	GRCh38
NC_000005.9:g.89999392G>T , CM000667.1:g.89999392G>T	GRCh37
NC_000005.8:g.90035148G>T	NCBI36
NG_007083.1:g.149776G>T
NG_007083.2:g.179232G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8156-90G>T MANE Select	ENSP00000384582.2:n.8156-90G>T
ENST00000639431.1:c.265+27366G>T	ENSP00000491057.1:n.265+27366G>T
ENST00000639473.1:n.3615-90G>T
ENST00000640012.1:c.1963-90G>T
ENST00000640374.1:n.1300-90G>T
ENST00000640403.1:c.5447-90G>T	ENSP00000492531.1:n.5447-90G>T
ENST00000640779.1:c.2885-90G>T
ENST00000405460.6:c.8156-90G>T	ENSP00000384582.2:n.8156-90G>T
ENST00000509621.1:c.853-90G>T
NM_032119.3:c.8156-90G>T	NP_115495.3:n.8156-90G>T
NR_003149.1:n.8169-90G>T
XM_011543675.1:c.8153-90G>T	XP_011541977.1:n.8153-90G>T
XM_011543676.1:c.8075-90G>T	XP_011541978.1:n.8075-90G>T
XM_011543677.1:c.5459-90G>T	XP_011541979.1:n.5459-90G>T
XM_011543678.1:c.8156-90G>T	XP_011541980.1:n.8156-90G>T
XM_011543679.1:c.8156-90G>T	XP_011541981.1:n.8156-90G>T
NM_032119.4:c.8156-90G>T MANE Select	NP_115495.3:n.8156-90G>T
XM_017009963.2:c.8156-90G>T	XP_016865452.1:n.8156-90G>T
XM_017009964.2:c.8153-90G>T	XP_016865453.1:n.8153-90G>T
XM_017009965.1:c.8153-90G>T	XP_016865454.1:n.8153-90G>T
XM_017009966.2:c.8075-90G>T	XP_016865455.1:n.8075-90G>T
XM_017009967.1:c.8060-90G>T	XP_016865456.1:n.8060-90G>T
XM_017009968.2:c.8156-90G>T	XP_016865457.1:n.8156-90G>T
XM_017009969.2:c.8156-90G>T	XP_016865458.1:n.8156-90G>T
XM_017009970.2:c.8156-90G>T	XP_016865459.1:n.8156-90G>T
XM_017009971.2:c.8156-90G>T	XP_016865460.1:n.8156-90G>T
XM_017009972.1:c.1274-90G>T	XP_016865461.1:n.1274-90G>T
XM_017009973.1:c.1274-90G>T	XP_016865462.1:n.1274-90G>T
XM_017009974.2:c.8156-90G>T	XP_016865463.1:n.8156-90G>T
NR_003149.2:n.8172-90G>T