Canonical Allele Identifier: CA1563051736

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91128362_91128365delinsTTTA , CM000667.2:g.91128362_91128365delinsTTTA	GRCh38
NC_000005.9:g.90424179_90424182delinsTTTA , CM000667.1:g.90424179_90424182delinsTTTA	GRCh37
NC_000005.8:g.90459935_90459938delinsTTTA	NCBI36
NG_007083.1:g.574563_574566delinsTTTA
NG_007083.2:g.604019_604022delinsTTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.18433-21668_18433-21665delinsTTTA MANE Select	ENSP00000384582.2:n.18433-21668_18433-21665delinsTTTA
ENST00000425867.3:c.7387-21668_7387-21665delinsTTTA	ENSP00000392618.3:n.7387-21668_7387-21665delinsTTTA
ENST00000638510.1:n.5700-21668_5700-21665delinsTTTA
ENST00000638990.1:c.1645-21668_1645-21665delinsTTTA
ENST00000639212.1:n.353-21668_353-21665delinsTTTA
ENST00000639530.1:n.301-21668_301-21665delinsTTTA
ENST00000639821.1:c.516+26022_516+26025delinsTTTA	ENSP00000492216.1:n.516+26022_516+26025delinsTTTA
ENST00000640256.1:n.301-24859_301-24856delinsTTTA
ENST00000640407.1:c.4882-21668_4882-21665delinsTTTA	ENSP00000491425.1:n.4882-21668_4882-21665delinsTTTA
ENST00000640815.1:c.517-21668_517-21665delinsTTTA	ENSP00000491767.1:n.517-21668_517-21665delinsTTTA
ENST00000405460.6:c.18433-21668_18433-21665delinsTTTA	ENSP00000384582.2:n.18433-21668_18433-21665delinsTTTA
ENST00000425867.2:c.5416-21668_5416-21665delinsTTTA	ENSP00000392618.2:n.5416-21668_5416-21665delinsTTTA
NM_032119.3:c.18433-21668_18433-21665delinsTTTA	NP_115495.3:n.18433-21668_18433-21665delinsTTTA
NR_003149.1:n.18446-21668_18446-21665delinsTTTA
XM_011543675.1:c.18430-21668_18430-21665delinsTTTA	XP_011541977.1:n.18430-21668_18430-21665delinsTTTA
XM_011543676.1:c.18352-21668_18352-21665delinsTTTA	XP_011541978.1:n.18352-21668_18352-21665delinsTTTA
XM_011543677.1:c.15736-21668_15736-21665delinsTTTA	XP_011541979.1:n.15736-21668_15736-21665delinsTTTA
NM_032119.4:c.18433-21668_18433-21665delinsTTTA MANE Select	NP_115495.3:n.18433-21668_18433-21665delinsTTTA
XM_017009963.2:c.18454-21668_18454-21665delinsTTTA	XP_016865452.1:n.18454-21668_18454-21665delinsTTTA
XM_017009964.2:c.18451-21668_18451-21665delinsTTTA	XP_016865453.1:n.18451-21668_18451-21665delinsTTTA
XM_017009965.1:c.18451-21668_18451-21665delinsTTTA	XP_016865454.1:n.18451-21668_18451-21665delinsTTTA
XM_017009966.2:c.18373-21668_18373-21665delinsTTTA	XP_016865455.1:n.18373-21668_18373-21665delinsTTTA
XM_017009967.1:c.18358-21668_18358-21665delinsTTTA	XP_016865456.1:n.18358-21668_18358-21665delinsTTTA
XM_017009968.2:c.18274-21668_18274-21665delinsTTTA	XP_016865457.1:n.18274-21668_18274-21665delinsTTTA
XM_017009969.2:c.18453+26022_18453+26025delinsTTTA	XP_016865458.1:n.18453+26022_18453+26025delinsTTTA
XM_017009972.1:c.11572-21668_11572-21665delinsTTTA	XP_016865461.1:n.11572-21668_11572-21665delinsTTTA
XM_017009973.1:c.11551-21668_11551-21665delinsTTTA	XP_016865462.1:n.11551-21668_11551-21665delinsTTTA
NR_003149.2:n.18449-21668_18449-21665delinsTTTA