Canonical Allele Identifier: CA247473

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90840711C>T , CM000667.2:g.90840711C>T	GRCh38
NC_000005.9:g.90136528C>T , CM000667.1:g.90136528C>T	GRCh37
NC_000005.8:g.90172284C>T	NCBI36
NG_007083.1:g.286912C>T
NG_007083.2:g.316368C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.16745C>T MANE Select	NP_115495.3:p.Thr5582Met
ENST00000405460.9:c.16745C>T MANE Select	ENSP00000384582.2:p.Thr5582Met
NM_032119.3:c.16745C>T	NP_115495.3:p.Thr5582Met
NR_003149.1:n.16758C>T
NR_003149.2:n.16761C>T
ENST00000405460.6:c.16745C>T	ENSP00000384582.2:p.Thr5582Met
ENST00000425867.2:c.3728C>T	ENSP00000392618.2:p.Thr1243Met
ENST00000425867.3:c.5699C>T	ENSP00000392618.3:p.Thr1900Met
ENST00000638510.1:n.4012C>T
ENST00000639431.1:c.266-144633C>T	ENSP00000491057.1:n.266-144633C>T
ENST00000640061.1:n.262C>T
ENST00000640407.1:c.3194C>T	ENSP00000491425.1:n.3194C>T
XM_011543675.1:c.16742C>T	XP_011541977.1:p.Thr5581Met
XM_011543676.1:c.16664C>T	XP_011541978.1:p.Thr5555Met
XM_011543677.1:c.14048C>T	XP_011541979.1:p.Thr4683Met
XM_017009963.2:c.16766C>T	XP_016865452.1:p.Thr5589Met
XM_017009964.2:c.16763C>T	XP_016865453.1:p.Thr5588Met
XM_017009965.1:c.16763C>T	XP_016865454.1:p.Thr5588Met
XM_017009966.2:c.16685C>T	XP_016865455.1:p.Thr5562Met
XM_017009967.1:c.16670C>T	XP_016865456.1:p.Thr5557Met
XM_017009968.2:c.16586C>T	XP_016865457.1:p.Thr5529Met
XM_017009969.2:c.16766C>T	XP_016865458.1:p.Thr5589Met
XM_017009972.1:c.9884C>T	XP_016865461.1:p.Thr3295Met
XM_017009973.1:c.9863C>T	XP_016865462.1:p.Thr3288Met