Canonical Allele Identifier: CA3339464

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90674142G>C , CM000667.2:g.90674142G>C	GRCh38
NC_000005.9:g.89969959G>C , CM000667.1:g.89969959G>C	GRCh37
NC_000005.8:g.90005715G>C	NCBI36
NG_007083.1:g.120343G>C
NG_007083.2:g.149799G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5018G>C MANE Select	NP_115495.3:p.Gly1673Ala
ENST00000405460.9:c.5018G>C MANE Select	ENSP00000384582.2:p.Gly1673Ala
NM_032119.3:c.5018G>C	NP_115495.3:p.Gly1673Ala
NR_003149.1:n.5114G>C
NR_003149.2:n.5117G>C
ENST00000405460.6:c.5018G>C	ENSP00000384582.2:p.Gly1673Ala
ENST00000450321.2:n.353G>C
ENST00000639473.1:n.477G>C
ENST00000639676.1:n.2616G>C
ENST00000640403.1:c.2309G>C	ENSP00000492531.1:p.Gly770Ala
XM_011543675.1:c.5018G>C	XP_011541977.1:p.Gly1673Ala
XM_011543676.1:c.5018G>C	XP_011541978.1:p.Gly1673Ala
XM_011543677.1:c.2321G>C	XP_011541979.1:p.Gly774Ala
XM_011543678.1:c.5018G>C	XP_011541980.1:p.Gly1673Ala
XM_011543679.1:c.5018G>C	XP_011541981.1:p.Gly1673Ala
XM_017009963.2:c.5018G>C	XP_016865452.1:p.Gly1673Ala
XM_017009964.2:c.5018G>C	XP_016865453.1:p.Gly1673Ala
XM_017009965.1:c.5015G>C	XP_016865454.1:p.Gly1672Ala
XM_017009966.2:c.5018G>C	XP_016865455.1:p.Gly1673Ala
XM_017009967.1:c.4922G>C	XP_016865456.1:p.Gly1641Ala
XM_017009968.2:c.5018G>C	XP_016865457.1:p.Gly1673Ala
XM_017009969.2:c.5018G>C	XP_016865458.1:p.Gly1673Ala
XM_017009970.2:c.5018G>C	XP_016865459.1:p.Gly1673Ala
XM_017009971.2:c.5018G>C	XP_016865460.1:p.Gly1673Ala
XM_017009974.2:c.5018G>C	XP_016865463.1:p.Gly1673Ala