Canonical Allele Identifier: CA360382261

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90694641G>T , CM000667.2:g.90694641G>T	GRCh38
NC_000005.9:g.89990458G>T , CM000667.1:g.89990458G>T	GRCh37
NC_000005.8:g.90026214G>T	NCBI36
NG_007083.1:g.140842G>T
NG_007083.2:g.170298G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.7885G>T MANE Select	NP_115495.3:p.Gly2629Ter
ENST00000405460.9:c.7885G>T MANE Select	ENSP00000384582.2:p.Gly2629Ter
NM_032119.3:c.7885G>T	NP_115495.3:p.Gly2629Ter
NR_003149.1:n.7898G>T
NR_003149.2:n.7901G>T
ENST00000405460.6:c.7885G>T	ENSP00000384582.2:p.Gly2629Ter
ENST00000509621.1:c.582G>T
ENST00000639431.1:c.265+18432G>T	ENSP00000491057.1:n.265+18432G>T
ENST00000639473.1:n.3344G>T
ENST00000640012.1:c.1692G>T
ENST00000640374.1:n.1029G>T
ENST00000640403.1:c.5176G>T	ENSP00000492531.1:p.Gly1726Ter
ENST00000640779.1:c.2614G>T
XM_011543675.1:c.7882G>T	XP_011541977.1:p.Gly2628Ter
XM_011543676.1:c.7804G>T	XP_011541978.1:p.Gly2602Ter
XM_011543677.1:c.5188G>T	XP_011541979.1:p.Gly1730Ter
XM_011543678.1:c.7885G>T	XP_011541980.1:p.Gly2629Ter
XM_011543679.1:c.7885G>T	XP_011541981.1:p.Gly2629Ter
XM_017009963.2:c.7885G>T	XP_016865452.1:p.Gly2629Ter
XM_017009964.2:c.7882G>T	XP_016865453.1:p.Gly2628Ter
XM_017009965.1:c.7882G>T	XP_016865454.1:p.Gly2628Ter
XM_017009966.2:c.7804G>T	XP_016865455.1:p.Gly2602Ter
XM_017009967.1:c.7789G>T	XP_016865456.1:p.Gly2597Ter
XM_017009968.2:c.7885G>T	XP_016865457.1:p.Gly2629Ter
XM_017009969.2:c.7885G>T	XP_016865458.1:p.Gly2629Ter
XM_017009970.2:c.7885G>T	XP_016865459.1:p.Gly2629Ter
XM_017009971.2:c.7885G>T	XP_016865460.1:p.Gly2629Ter
XM_017009972.1:c.1003G>T	XP_016865461.1:p.Gly335Ter
XM_017009973.1:c.1003G>T	XP_016865462.1:p.Gly335Ter
XM_017009974.2:c.7885G>T	XP_016865463.1:p.Gly2629Ter