Canonical Allele Identifier: CA360431834

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91072544C>T , CM000667.2:g.91072544C>T	GRCh38
NC_000005.9:g.90368361C>T , CM000667.1:g.90368361C>T	GRCh37
NC_000005.8:g.90404117C>T	NCBI36
NG_007083.1:g.518745C>T
NG_007083.2:g.548201C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18250C>T MANE Select	NP_115495.3:p.Gln6084Ter
ENST00000405460.9:c.18250C>T MANE Select	ENSP00000384582.2:p.Gln6084Ter
NM_032119.3:c.18250C>T	NP_115495.3:p.Gln6084Ter
NR_003149.1:n.18263C>T
NR_003149.2:n.18266C>T
ENST00000405460.6:c.18250C>T	ENSP00000384582.2:p.Gln6084Ter
ENST00000425867.2:c.5233C>T	ENSP00000392618.2:p.Gln1745Ter
ENST00000425867.3:c.7204C>T	ENSP00000392618.3:p.Gln2402Ter
ENST00000638510.1:n.5517C>T
ENST00000638990.1:c.1462C>T
ENST00000639431.1:c.542C>T	ENSP00000491057.1:n.542C>T
ENST00000639707.1:c.334C>T	ENSP00000492328.1:p.Gln112Ter
ENST00000639821.1:c.334C>T	ENSP00000492216.1:p.Gln112Ter
ENST00000640369.1:c.334C>T	ENSP00000491401.1:p.Gln112Ter
ENST00000640407.1:c.4699C>T	ENSP00000491425.1:n.4699C>T
ENST00000640815.1:c.334C>T	ENSP00000491767.1:p.Gln112Ter
XM_011543675.1:c.18247C>T	XP_011541977.1:p.Gln6083Ter
XM_011543676.1:c.18169C>T	XP_011541978.1:p.Gln6057Ter
XM_011543677.1:c.15553C>T	XP_011541979.1:p.Gln5185Ter
XM_017009963.2:c.18271C>T	XP_016865452.1:p.Gln6091Ter
XM_017009964.2:c.18268C>T	XP_016865453.1:p.Gln6090Ter
XM_017009965.1:c.18268C>T	XP_016865454.1:p.Gln6090Ter
XM_017009966.2:c.18190C>T	XP_016865455.1:p.Gln6064Ter
XM_017009967.1:c.18175C>T	XP_016865456.1:p.Gln6059Ter
XM_017009968.2:c.18091C>T	XP_016865457.1:p.Gln6031Ter
XM_017009969.2:c.18271C>T	XP_016865458.1:p.Gln6091Ter
XM_017009972.1:c.11389C>T	XP_016865461.1:p.Gln3797Ter
XM_017009973.1:c.11368C>T	XP_016865462.1:p.Gln3790Ter