Canonical Allele Identifier: CA360399161

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90085661A>T (hg19) ; chr5:g.90789844A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90789844A>T , CM000667.2:g.90789844A>T	GRCh38
NC_000005.9:g.90085661A>T , CM000667.1:g.90085661A>T	GRCh37
NC_000005.8:g.90121417A>T	NCBI36
NG_007083.1:g.236045A>T
NG_007083.2:g.265501A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14036A>T MANE Select	ENSP00000384582.2:p.Glu4679Val
ENST00000425867.3:c.2990A>T	ENSP00000392618.3:p.Glu997Val
ENST00000638510.1:n.1303A>T
ENST00000638975.1:c.665A>T	ENSP00000492630.1:p.Glu222Val
ENST00000639431.1:c.265+113635A>T	ENSP00000491057.1:n.265+113635A>T
ENST00000640407.1:c.446A>T	ENSP00000491425.1:p.Glu149Val
ENST00000405460.6:c.14036A>T	ENSP00000384582.2:p.Glu4679Val
ENST00000425867.2:c.1019A>T	ENSP00000392618.2:p.Glu340Val
NM_032119.3:c.14036A>T	NP_115495.3:p.Glu4679Val
NR_003149.1:n.14049A>T
XM_011543675.1:c.14033A>T	XP_011541977.1:p.Glu4678Val
XM_011543676.1:c.13955A>T	XP_011541978.1:p.Glu4652Val
XM_011543677.1:c.11339A>T	XP_011541979.1:p.Glu3780Val
XM_011543678.1:c.14036A>T	XP_011541980.1:p.Glu4679Val
NM_032119.4:c.14036A>T MANE Select	NP_115495.3:p.Glu4679Val
XM_017009963.2:c.14057A>T	XP_016865452.1:p.Glu4686Val
XM_017009964.2:c.14054A>T	XP_016865453.1:p.Glu4685Val
XM_017009965.1:c.14054A>T	XP_016865454.1:p.Glu4685Val
XM_017009966.2:c.13976A>T	XP_016865455.1:p.Glu4659Val
XM_017009967.1:c.13961A>T	XP_016865456.1:p.Glu4654Val
XM_017009968.2:c.14057A>T	XP_016865457.1:p.Glu4686Val
XM_017009969.2:c.14057A>T	XP_016865458.1:p.Glu4686Val
XM_017009970.2:c.14057A>T	XP_016865459.1:p.Glu4686Val
XM_017009971.2:c.14057A>T	XP_016865460.1:p.Glu4686Val
XM_017009972.1:c.7175A>T	XP_016865461.1:p.Glu2392Val
XM_017009973.1:c.7154A>T	XP_016865462.1:p.Glu2385Val
NR_003149.2:n.14052A>T