Canonical Allele Identifier: CA360401079

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791082G>T , CM000667.2:g.90791082G>T	GRCh38
NC_000005.9:g.90086899G>T , CM000667.1:g.90086899G>T	GRCh37
NC_000005.8:g.90122655G>T	NCBI36
NG_007083.1:g.237283G>T
NG_007083.2:g.266739G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.14253G>T MANE Select	NP_115495.3:p.Trp4751Cys
ENST00000405460.9:c.14253G>T MANE Select	ENSP00000384582.2:p.Trp4751Cys
NM_032119.3:c.14253G>T	NP_115495.3:p.Trp4751Cys
NR_003149.1:n.14266G>T
NR_003149.2:n.14269G>T
ENST00000405460.6:c.14253G>T	ENSP00000384582.2:p.Trp4751Cys
ENST00000425867.2:c.1236G>T	ENSP00000392618.2:p.Trp412Cys
ENST00000425867.3:c.3207G>T	ENSP00000392618.3:p.Trp1069Cys
ENST00000638510.1:n.1520G>T
ENST00000638585.1:n.19G>T
ENST00000638975.1:c.882G>T	ENSP00000492630.1:p.Trp294Cys
ENST00000639431.1:c.265+114873G>T	ENSP00000491057.1:n.265+114873G>T
ENST00000640407.1:c.663G>T	ENSP00000491425.1:p.Trp221Cys
XM_011543675.1:c.14250G>T	XP_011541977.1:p.Trp4750Cys
XM_011543676.1:c.14172G>T	XP_011541978.1:p.Trp4724Cys
XM_011543677.1:c.11556G>T	XP_011541979.1:p.Trp3852Cys
XM_011543678.1:c.14253G>T	XP_011541980.1:p.Trp4751Cys
XM_017009963.2:c.14274G>T	XP_016865452.1:p.Trp4758Cys
XM_017009964.2:c.14271G>T	XP_016865453.1:p.Trp4757Cys
XM_017009965.1:c.14271G>T	XP_016865454.1:p.Trp4757Cys
XM_017009966.2:c.14193G>T	XP_016865455.1:p.Trp4731Cys
XM_017009967.1:c.14178G>T	XP_016865456.1:p.Trp4726Cys
XM_017009968.2:c.14274G>T	XP_016865457.1:p.Trp4758Cys
XM_017009969.2:c.14274G>T	XP_016865458.1:p.Trp4758Cys
XM_017009970.2:c.14274G>T	XP_016865459.1:p.Trp4758Cys
XM_017009971.2:c.14274G>T	XP_016865460.1:p.Trp4758Cys
XM_017009972.1:c.7392G>T	XP_016865461.1:p.Trp2464Cys
XM_017009973.1:c.7371G>T	XP_016865462.1:p.Trp2457Cys