Canonical Allele Identifier: CA445467523

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086935A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791118A>T , CM000667.2:g.90791118A>T	GRCh38
NC_000005.9:g.90086935A>T , CM000667.1:g.90086935A>T	GRCh37
NC_000005.8:g.90122691A>T	NCBI36
NG_007083.1:g.237319A>T
NG_007083.2:g.266775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14289A>T MANE Select	ENSP00000384582.2:p.Val4763=
ENST00000425867.3:c.3243A>T	ENSP00000392618.3:p.Val1081=
ENST00000638510.1:n.1556A>T
ENST00000638585.1:n.55A>T
ENST00000638975.1:c.918A>T	ENSP00000492630.1:p.Val306=
ENST00000639431.1:c.265+114909A>T	ENSP00000491057.1:n.265+114909A>T
ENST00000640407.1:c.699A>T	ENSP00000491425.1:p.Val233=
ENST00000405460.6:c.14289A>T	ENSP00000384582.2:p.Val4763=
ENST00000425867.2:c.1272A>T	ENSP00000392618.2:p.Val424=
NM_032119.3:c.14289A>T	NP_115495.3:p.Val4763=
NR_003149.1:n.14302A>T
XM_011543675.1:c.14286A>T	XP_011541977.1:p.Val4762=
XM_011543676.1:c.14208A>T	XP_011541978.1:p.Val4736=
XM_011543677.1:c.11592A>T	XP_011541979.1:p.Val3864=
XM_011543678.1:c.14289A>T	XP_011541980.1:p.Val4763=
NM_032119.4:c.14289A>T MANE Select	NP_115495.3:p.Val4763=
XM_017009963.2:c.14310A>T	XP_016865452.1:p.Val4770=
XM_017009964.2:c.14307A>T	XP_016865453.1:p.Val4769=
XM_017009965.1:c.14307A>T	XP_016865454.1:p.Val4769=
XM_017009966.2:c.14229A>T	XP_016865455.1:p.Val4743=
XM_017009967.1:c.14214A>T	XP_016865456.1:p.Val4738=
XM_017009968.2:c.14310A>T	XP_016865457.1:p.Val4770=
XM_017009969.2:c.14310A>T	XP_016865458.1:p.Val4770=
XM_017009970.2:c.14310A>T	XP_016865459.1:p.Val4770=
XM_017009971.2:c.14310A>T	XP_016865460.1:p.Val4770=
XM_017009972.1:c.7428A>T	XP_016865461.1:p.Val2476=
XM_017009973.1:c.7407A>T	XP_016865462.1:p.Val2469=
NR_003149.2:n.14305A>T