Canonical Allele Identifier: CA3342499

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965449A>C , CM000667.2:g.90965449A>C	GRCh38
NC_000005.9:g.90261266A>C , CM000667.1:g.90261266A>C	GRCh37
NC_000005.8:g.90297022A>C	NCBI36
NG_007083.1:g.411650A>C
NG_007083.2:g.441106A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.17891A>C MANE Select	NP_115495.3:p.Gln5964Pro
ENST00000405460.9:c.17891A>C MANE Select	ENSP00000384582.2:p.Gln5964Pro
NM_032119.3:c.17891A>C	NP_115495.3:p.Gln5964Pro
NR_003149.1:n.17904A>C
NR_003149.2:n.17907A>C
ENST00000405460.6:c.17891A>C	ENSP00000384582.2:p.Gln5964Pro
ENST00000425867.2:c.4874A>C	ENSP00000392618.2:p.Gln1625Pro
ENST00000425867.3:c.6845A>C	ENSP00000392618.3:p.Gln2282Pro
ENST00000638510.1:n.5158A>C
ENST00000638990.1:c.1103A>C
ENST00000639431.1:c.266-19895A>C	ENSP00000491057.1:n.266-19895A>C
ENST00000639707.1:c.-26A>C	ENSP00000492328.1:n.-26A>C
ENST00000639821.1:c.-26A>C	ENSP00000492216.1:n.-26A>C
ENST00000640369.1:c.-26A>C	ENSP00000491401.1:n.-26A>C
ENST00000640407.1:c.4340A>C	ENSP00000491425.1:n.4340A>C
ENST00000640815.1:c.-26A>C	ENSP00000491767.1:n.-26A>C
XM_011543675.1:c.17888A>C	XP_011541977.1:p.Gln5963Pro
XM_011543676.1:c.17810A>C	XP_011541978.1:p.Gln5937Pro
XM_011543677.1:c.15194A>C	XP_011541979.1:p.Gln5065Pro
XM_017009963.2:c.17912A>C	XP_016865452.1:p.Gln5971Pro
XM_017009964.2:c.17909A>C	XP_016865453.1:p.Gln5970Pro
XM_017009965.1:c.17909A>C	XP_016865454.1:p.Gln5970Pro
XM_017009966.2:c.17831A>C	XP_016865455.1:p.Gln5944Pro
XM_017009967.1:c.17816A>C	XP_016865456.1:p.Gln5939Pro
XM_017009968.2:c.17732A>C	XP_016865457.1:p.Gln5911Pro
XM_017009969.2:c.17912A>C	XP_016865458.1:p.Gln5971Pro
XM_017009972.1:c.11030A>C	XP_016865461.1:p.Gln3677Pro
XM_017009973.1:c.11009A>C	XP_016865462.1:p.Gln3670Pro