Canonical Allele Identifier: CA445468391

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89990145G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90694328G>T , CM000667.2:g.90694328G>T	GRCh38
NC_000005.9:g.89990145G>T , CM000667.1:g.89990145G>T	GRCh37
NC_000005.8:g.90025901G>T	NCBI36
NG_007083.1:g.140529G>T
NG_007083.2:g.169985G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7572G>T MANE Select	ENSP00000384582.2:p.Val2524=
ENST00000639431.1:c.265+18119G>T	ENSP00000491057.1:n.265+18119G>T
ENST00000639473.1:n.3031G>T
ENST00000640012.1:c.1379G>T
ENST00000640374.1:n.716G>T
ENST00000640403.1:c.4863G>T	ENSP00000492531.1:p.Val1621=
ENST00000640779.1:c.2301G>T
ENST00000405460.6:c.7572G>T	ENSP00000384582.2:p.Val2524=
ENST00000509621.1:c.269G>T
NM_032119.3:c.7572G>T	NP_115495.3:p.Val2524=
NR_003149.1:n.7585G>T
XM_011543675.1:c.7569G>T	XP_011541977.1:p.Val2523=
XM_011543676.1:c.7491G>T	XP_011541978.1:p.Val2497=
XM_011543677.1:c.4875G>T	XP_011541979.1:p.Val1625=
XM_011543678.1:c.7572G>T	XP_011541980.1:p.Val2524=
XM_011543679.1:c.7572G>T	XP_011541981.1:p.Val2524=
NM_032119.4:c.7572G>T MANE Select	NP_115495.3:p.Val2524=
XM_017009963.2:c.7572G>T	XP_016865452.1:p.Val2524=
XM_017009964.2:c.7569G>T	XP_016865453.1:p.Val2523=
XM_017009965.1:c.7569G>T	XP_016865454.1:p.Val2523=
XM_017009966.2:c.7491G>T	XP_016865455.1:p.Val2497=
XM_017009967.1:c.7476G>T	XP_016865456.1:p.Val2492=
XM_017009968.2:c.7572G>T	XP_016865457.1:p.Val2524=
XM_017009969.2:c.7572G>T	XP_016865458.1:p.Val2524=
XM_017009970.2:c.7572G>T	XP_016865459.1:p.Val2524=
XM_017009971.2:c.7572G>T	XP_016865460.1:p.Val2524=
XM_017009972.1:c.690G>T	XP_016865461.1:p.Val230=
XM_017009973.1:c.690G>T	XP_016865462.1:p.Val230=
XM_017009974.2:c.7572G>T	XP_016865463.1:p.Val2524=
NR_003149.2:n.7588G>T