Canonical Allele Identifier: CA445410448

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89940590A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644773A>G , CM000667.2:g.90644773A>G	GRCh38
NC_000005.9:g.89940590A>G , CM000667.1:g.89940590A>G	GRCh37
NC_000005.8:g.89976346A>G	NCBI36
NG_007083.1:g.90974A>G
NG_007083.2:g.120430A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2802A>G MANE Select	ENSP00000384582.2:p.Pro934=
ENST00000504142.2:n.1568A>G
ENST00000639676.1:n.400A>G
ENST00000640403.1:c.105A>G	ENSP00000492531.1:p.Pro35=
ENST00000405460.6:c.2802A>G	ENSP00000384582.2:p.Pro934=
ENST00000504142.1:c.1567A>G
NM_032119.3:c.2802A>G	NP_115495.3:p.Pro934=
NR_003149.1:n.2898A>G
XM_011543675.1:c.2802A>G	XP_011541977.1:p.Pro934=
XM_011543676.1:c.2802A>G	XP_011541978.1:p.Pro934=
XM_011543677.1:c.105A>G	XP_011541979.1:p.Pro35=
XM_011543678.1:c.2802A>G	XP_011541980.1:p.Pro934=
XM_011543679.1:c.2802A>G	XP_011541981.1:p.Pro934=
NM_032119.4:c.2802A>G MANE Select	NP_115495.3:p.Pro934=
XM_017009963.2:c.2802A>G	XP_016865452.1:p.Pro934=
XM_017009964.2:c.2802A>G	XP_016865453.1:p.Pro934=
XM_017009965.1:c.2799A>G	XP_016865454.1:p.Pro933=
XM_017009966.2:c.2802A>G	XP_016865455.1:p.Pro934=
XM_017009967.1:c.2706A>G	XP_016865456.1:p.Pro902=
XM_017009968.2:c.2802A>G	XP_016865457.1:p.Pro934=
XM_017009969.2:c.2802A>G	XP_016865458.1:p.Pro934=
XM_017009970.2:c.2802A>G	XP_016865459.1:p.Pro934=
XM_017009971.2:c.2802A>G	XP_016865460.1:p.Pro934=
XM_017009974.2:c.2802A>G	XP_016865463.1:p.Pro934=
NR_003149.2:n.2901A>G