Canonical Allele Identifier: CA176227

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90776555A>G , CM000667.2:g.90776555A>G	GRCh38
NC_000005.9:g.90072372A>G , CM000667.1:g.90072372A>G	GRCh37
NC_000005.8:g.90108128A>G	NCBI36
NG_007083.1:g.222756A>G
NG_007083.2:g.252212A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12506A>G MANE Select	NP_115495.3:p.Tyr4169Cys
ENST00000405460.9:c.12506A>G MANE Select	ENSP00000384582.2:p.Tyr4169Cys
NM_032119.3:c.12506A>G	NP_115495.3:p.Tyr4169Cys
NR_003149.1:n.12519A>G
NR_003149.2:n.12522A>G
ENST00000405460.6:c.12506A>G	ENSP00000384582.2:p.Tyr4169Cys
ENST00000425867.3:c.1460A>G	ENSP00000392618.3:p.Tyr487Cys
ENST00000639431.1:c.265+100346A>G	ENSP00000491057.1:n.265+100346A>G
ENST00000640464.1:n.2925A>G
ENST00000640729.1:n.1083A>G
XM_011543675.1:c.12503A>G	XP_011541977.1:p.Tyr4168Cys
XM_011543676.1:c.12425A>G	XP_011541978.1:p.Tyr4142Cys
XM_011543677.1:c.9809A>G	XP_011541979.1:p.Tyr3270Cys
XM_011543678.1:c.12506A>G	XP_011541980.1:p.Tyr4169Cys
XM_017009963.2:c.12527A>G	XP_016865452.1:p.Tyr4176Cys
XM_017009964.2:c.12524A>G	XP_016865453.1:p.Tyr4175Cys
XM_017009965.1:c.12524A>G	XP_016865454.1:p.Tyr4175Cys
XM_017009966.2:c.12446A>G	XP_016865455.1:p.Tyr4149Cys
XM_017009967.1:c.12431A>G	XP_016865456.1:p.Tyr4144Cys
XM_017009968.2:c.12527A>G	XP_016865457.1:p.Tyr4176Cys
XM_017009969.2:c.12527A>G	XP_016865458.1:p.Tyr4176Cys
XM_017009970.2:c.12527A>G	XP_016865459.1:p.Tyr4176Cys
XM_017009971.2:c.12527A>G	XP_016865460.1:p.Tyr4176Cys
XM_017009972.1:c.5645A>G	XP_016865461.1:p.Tyr1882Cys
XM_017009973.1:c.5624A>G	XP_016865462.1:p.Tyr1875Cys