Canonical Allele Identifier: CA360371805

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988568A>C (hg19) ; chr5:g.90692751A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692751A>C , CM000667.2:g.90692751A>C	GRCh38
NC_000005.9:g.89988568A>C , CM000667.1:g.89988568A>C	GRCh37
NC_000005.8:g.90024324A>C	NCBI36
NG_007083.1:g.138952A>C
NG_007083.2:g.168408A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7098A>C MANE Select	ENSP00000384582.2:p.Glu2366Asp
ENST00000639431.1:c.265+16542A>C	ENSP00000491057.1:n.265+16542A>C
ENST00000639473.1:n.2557A>C
ENST00000640012.1:c.905A>C
ENST00000640374.1:n.242A>C
ENST00000640403.1:c.4389A>C	ENSP00000492531.1:p.Glu1463Asp
ENST00000640779.1:c.1827A>C
ENST00000405460.6:c.7098A>C	ENSP00000384582.2:p.Glu2366Asp
NM_032119.3:c.7098A>C	NP_115495.3:p.Glu2366Asp
NR_003149.1:n.7111A>C
XM_011543675.1:c.7095A>C	XP_011541977.1:p.Glu2365Asp
XM_011543676.1:c.7017A>C	XP_011541978.1:p.Glu2339Asp
XM_011543677.1:c.4401A>C	XP_011541979.1:p.Glu1467Asp
XM_011543678.1:c.7098A>C	XP_011541980.1:p.Glu2366Asp
XM_011543679.1:c.7098A>C	XP_011541981.1:p.Glu2366Asp
NM_032119.4:c.7098A>C MANE Select	NP_115495.3:p.Glu2366Asp
XM_017009963.2:c.7098A>C	XP_016865452.1:p.Glu2366Asp
XM_017009964.2:c.7095A>C	XP_016865453.1:p.Glu2365Asp
XM_017009965.1:c.7095A>C	XP_016865454.1:p.Glu2365Asp
XM_017009966.2:c.7017A>C	XP_016865455.1:p.Glu2339Asp
XM_017009967.1:c.7002A>C	XP_016865456.1:p.Glu2334Asp
XM_017009968.2:c.7098A>C	XP_016865457.1:p.Glu2366Asp
XM_017009969.2:c.7098A>C	XP_016865458.1:p.Glu2366Asp
XM_017009970.2:c.7098A>C	XP_016865459.1:p.Glu2366Asp
XM_017009971.2:c.7098A>C	XP_016865460.1:p.Glu2366Asp
XM_017009972.1:c.216A>C	XP_016865461.1:p.Glu72Asp
XM_017009973.1:c.216A>C	XP_016865462.1:p.Glu72Asp
XM_017009974.2:c.7098A>C	XP_016865463.1:p.Glu2366Asp
NR_003149.2:n.7114A>C