Canonical Allele Identifier: CA3340435

Gene: ADGRV1

Linked Data

• dbSNP Id: rs760145754
• ExAC: 5:90008100 C / T
• gnomAD v2: 5-90008100-C-T
• gnomAD v3: 5-90712283-C-T
• gnomAD v4: 5-90712283-C-T
• MyVariant Identifiers: chr5:g.90008100C>T (hg19) ; chr5:g.90712283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712283C>T , CM000667.2:g.90712283C>T	GRCh38
NC_000005.9:g.90008100C>T , CM000667.1:g.90008100C>T	GRCh37
NC_000005.8:g.90043856C>T	NCBI36
NG_007083.1:g.158484C>T
NG_007083.2:g.187940C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9043-4C>T MANE Select	ENSP00000384582.2:n.9043-4C>T
ENST00000639431.1:c.265+36074C>T	ENSP00000491057.1:n.265+36074C>T
ENST00000639473.1:n.4502-4C>T
ENST00000640012.1:c.2850-4C>T
ENST00000640374.1:n.2187-4C>T
ENST00000640779.1:c.3772-4C>T
ENST00000405460.6:c.9043-4C>T	ENSP00000384582.2:n.9043-4C>T
ENST00000509621.1:c.1740-4C>T
NM_032119.3:c.9043-4C>T	NP_115495.3:n.9043-4C>T
NR_003149.1:n.9056-4C>T
XM_011543675.1:c.9040-4C>T	XP_011541977.1:n.9040-4C>T
XM_011543676.1:c.8962-4C>T	XP_011541978.1:n.8962-4C>T
XM_011543677.1:c.6346-4C>T	XP_011541979.1:n.6346-4C>T
XM_011543678.1:c.9043-4C>T	XP_011541980.1:n.9043-4C>T
XM_011543679.1:c.9043-4C>T	XP_011541981.1:n.9043-4C>T
NM_032119.4:c.9043-4C>T MANE Select	NP_115495.3:n.9043-4C>T
XM_017009963.2:c.9064-4C>T	XP_016865452.1:n.9064-4C>T
XM_017009964.2:c.9061-4C>T	XP_016865453.1:n.9061-4C>T
XM_017009965.1:c.9061-4C>T	XP_016865454.1:n.9061-4C>T
XM_017009966.2:c.8983-4C>T	XP_016865455.1:n.8983-4C>T
XM_017009967.1:c.8968-4C>T	XP_016865456.1:n.8968-4C>T
XM_017009968.2:c.9064-4C>T	XP_016865457.1:n.9064-4C>T
XM_017009969.2:c.9064-4C>T	XP_016865458.1:n.9064-4C>T
XM_017009970.2:c.9064-4C>T	XP_016865459.1:n.9064-4C>T
XM_017009971.2:c.9064-4C>T	XP_016865460.1:n.9064-4C>T
XM_017009972.1:c.2182-4C>T	XP_016865461.1:n.2182-4C>T
XM_017009973.1:c.2161-4C>T	XP_016865462.1:n.2161-4C>T
XM_017009974.2:c.9064-4C>T	XP_016865463.1:n.9064-4C>T
NR_003149.2:n.9059-4C>T