Canonical Allele Identifier: CA2674569959

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712242-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712242A>T , CM000667.2:g.90712242A>T	GRCh38
NC_000005.9:g.90008059A>T , CM000667.1:g.90008059A>T	GRCh37
NC_000005.8:g.90043815A>T	NCBI36
NG_007083.1:g.158443A>T
NG_007083.2:g.187899A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9043-45A>T MANE Select	ENSP00000384582.2:n.9043-45A>T
ENST00000639431.1:c.265+36033A>T	ENSP00000491057.1:n.265+36033A>T
ENST00000639473.1:n.4502-45A>T
ENST00000640012.1:c.2850-45A>T
ENST00000640374.1:n.2187-45A>T
ENST00000640779.1:c.3772-45A>T
ENST00000405460.6:c.9043-45A>T	ENSP00000384582.2:n.9043-45A>T
ENST00000509621.1:c.1740-45A>T
NM_032119.3:c.9043-45A>T	NP_115495.3:n.9043-45A>T
NR_003149.1:n.9056-45A>T
XM_011543675.1:c.9040-45A>T	XP_011541977.1:n.9040-45A>T
XM_011543676.1:c.8962-45A>T	XP_011541978.1:n.8962-45A>T
XM_011543677.1:c.6346-45A>T	XP_011541979.1:n.6346-45A>T
XM_011543678.1:c.9043-45A>T	XP_011541980.1:n.9043-45A>T
XM_011543679.1:c.9043-45A>T	XP_011541981.1:n.9043-45A>T
NM_032119.4:c.9043-45A>T MANE Select	NP_115495.3:n.9043-45A>T
XM_017009963.2:c.9064-45A>T	XP_016865452.1:n.9064-45A>T
XM_017009964.2:c.9061-45A>T	XP_016865453.1:n.9061-45A>T
XM_017009965.1:c.9061-45A>T	XP_016865454.1:n.9061-45A>T
XM_017009966.2:c.8983-45A>T	XP_016865455.1:n.8983-45A>T
XM_017009967.1:c.8968-45A>T	XP_016865456.1:n.8968-45A>T
XM_017009968.2:c.9064-45A>T	XP_016865457.1:n.9064-45A>T
XM_017009969.2:c.9064-45A>T	XP_016865458.1:n.9064-45A>T
XM_017009970.2:c.9064-45A>T	XP_016865459.1:n.9064-45A>T
XM_017009971.2:c.9064-45A>T	XP_016865460.1:n.9064-45A>T
XM_017009972.1:c.2182-45A>T	XP_016865461.1:n.2182-45A>T
XM_017009973.1:c.2161-45A>T	XP_016865462.1:n.2161-45A>T
XM_017009974.2:c.9064-45A>T	XP_016865463.1:n.9064-45A>T
NR_003149.2:n.9059-45A>T