Canonical Allele Identifier: CA360431522

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91102303G>A , CM000667.2:g.91102303G>A	GRCh38
NC_000005.9:g.90398120G>A , CM000667.1:g.90398120G>A	GRCh37
NC_000005.8:g.90433876G>A	NCBI36
NG_007083.1:g.548504G>A
NG_007083.2:g.577960G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18395G>A MANE Select	NP_115495.3:p.Trp6132Ter
ENST00000405460.9:c.18395G>A MANE Select	ENSP00000384582.2:p.Trp6132Ter
NM_032119.3:c.18395G>A	NP_115495.3:p.Trp6132Ter
NR_003149.1:n.18408G>A
NR_003149.2:n.18411G>A
ENST00000405460.6:c.18395G>A	ENSP00000384582.2:p.Trp6132Ter
ENST00000425867.2:c.5378G>A	ENSP00000392618.2:p.Trp1793Ter
ENST00000425867.3:c.7349G>A	ENSP00000392618.3:p.Trp2450Ter
ENST00000638510.1:n.5662G>A
ENST00000638990.1:c.1607G>A
ENST00000639212.1:n.315G>A
ENST00000639530.1:n.263G>A
ENST00000639821.1:c.479G>A	ENSP00000492216.1:p.Trp160Ter
ENST00000640256.1:n.263G>A
ENST00000640407.1:c.4844G>A	ENSP00000491425.1:n.4844G>A
ENST00000640815.1:c.479G>A	ENSP00000491767.1:p.Trp160Ter
XM_011543675.1:c.18392G>A	XP_011541977.1:p.Trp6131Ter
XM_011543676.1:c.18314G>A	XP_011541978.1:p.Trp6105Ter
XM_011543677.1:c.15698G>A	XP_011541979.1:p.Trp5233Ter
XM_017009963.2:c.18416G>A	XP_016865452.1:p.Trp6139Ter
XM_017009964.2:c.18413G>A	XP_016865453.1:p.Trp6138Ter
XM_017009965.1:c.18413G>A	XP_016865454.1:p.Trp6138Ter
XM_017009966.2:c.18335G>A	XP_016865455.1:p.Trp6112Ter
XM_017009967.1:c.18320G>A	XP_016865456.1:p.Trp6107Ter
XM_017009968.2:c.18236G>A	XP_016865457.1:p.Trp6079Ter
XM_017009969.2:c.18416G>A	XP_016865458.1:p.Trp6139Ter
XM_017009972.1:c.11534G>A	XP_016865461.1:p.Trp3845Ter
XM_017009973.1:c.11513G>A	XP_016865462.1:p.Trp3838Ter