Canonical Allele Identifier: CA3341877

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810437G>T , CM000667.2:g.90810437G>T	GRCh38
NC_000005.9:g.90106254G>T , CM000667.1:g.90106254G>T	GRCh37
NC_000005.8:g.90142010G>T	NCBI36
NG_007083.1:g.256638G>T
NG_007083.2:g.286094G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.15177G>T MANE Select	NP_115495.3:p.Gln5059His
ENST00000405460.9:c.15177G>T MANE Select	ENSP00000384582.2:p.Gln5059His
NM_032119.3:c.15177G>T	NP_115495.3:p.Gln5059His
NR_003149.1:n.15190G>T
NR_003149.2:n.15193G>T
ENST00000405460.6:c.15177G>T	ENSP00000384582.2:p.Gln5059His
ENST00000425867.2:c.2160G>T	ENSP00000392618.2:p.Gln720His
ENST00000425867.3:c.4131G>T	ENSP00000392618.3:p.Gln1377His
ENST00000638510.1:n.2444G>T
ENST00000639431.1:c.265+134228G>T	ENSP00000491057.1:n.265+134228G>T
ENST00000640407.1:c.1587G>T	ENSP00000491425.1:p.Gln529His
XM_011543675.1:c.15174G>T	XP_011541977.1:p.Gln5058His
XM_011543676.1:c.15096G>T	XP_011541978.1:p.Gln5032His
XM_011543677.1:c.12480G>T	XP_011541979.1:p.Gln4160His
XM_017009963.2:c.15198G>T	XP_016865452.1:p.Gln5066His
XM_017009964.2:c.15195G>T	XP_016865453.1:p.Gln5065His
XM_017009965.1:c.15195G>T	XP_016865454.1:p.Gln5065His
XM_017009966.2:c.15117G>T	XP_016865455.1:p.Gln5039His
XM_017009967.1:c.15102G>T	XP_016865456.1:p.Gln5034His
XM_017009968.2:c.15018G>T	XP_016865457.1:p.Gln5006His
XM_017009969.2:c.15198G>T	XP_016865458.1:p.Gln5066His
XM_017009971.2:c.*131G>T	XP_016865460.1:n.*131G>T
XM_017009972.1:c.8316G>T	XP_016865461.1:p.Gln2772His
XM_017009973.1:c.8295G>T	XP_016865462.1:p.Gln2765His