Canonical Allele Identifier: CA3342777

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91163885C>T , CM000667.2:g.91163885C>T	GRCh38
NC_000005.9:g.90459702C>T , CM000667.1:g.90459702C>T	GRCh37
NC_000005.8:g.90495458C>T	NCBI36
NG_007083.1:g.610086C>T
NG_007083.2:g.639542C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18906C>T MANE Select	NP_115495.3:p.Ala6302=
ENST00000405460.9:c.18906C>T MANE Select	ENSP00000384582.2:p.Ala6302=
NM_032119.3:c.18906C>T	NP_115495.3:p.Ala6302=
NR_003149.1:n.18919C>T
NR_003149.2:n.18922C>T
ENST00000405460.6:c.18906C>T	ENSP00000384582.2:p.Ala6302=
ENST00000425867.2:c.5889C>T	ENSP00000392618.2:p.Ala1963=
ENST00000425867.3:c.7860C>T	ENSP00000392618.3:p.Ala2620=
ENST00000638510.1:n.6173C>T
ENST00000638990.1:c.2118C>T
ENST00000639212.1:n.826C>T
ENST00000639530.1:n.774C>T
ENST00000639821.1:c.*41C>T	ENSP00000492216.1:n.*41C>T
ENST00000640256.1:n.582C>T
ENST00000640407.1:c.5355C>T	ENSP00000491425.1:n.5355C>T
ENST00000640815.1:c.990C>T	ENSP00000491767.1:p.Ala330=
XM_011543675.1:c.18903C>T	XP_011541977.1:p.Ala6301=
XM_011543676.1:c.18825C>T	XP_011541978.1:p.Ala6275=
XM_011543677.1:c.16209C>T	XP_011541979.1:p.Ala5403=
XM_017009963.2:c.18927C>T	XP_016865452.1:p.Ala6309=
XM_017009964.2:c.18924C>T	XP_016865453.1:p.Ala6308=
XM_017009965.1:c.18924C>T	XP_016865454.1:p.Ala6308=
XM_017009966.2:c.18846C>T	XP_016865455.1:p.Ala6282=
XM_017009967.1:c.18831C>T	XP_016865456.1:p.Ala6277=
XM_017009968.2:c.18747C>T	XP_016865457.1:p.Ala6249=
XM_017009969.2:c.*41C>T	XP_016865458.1:n.*41C>T
XM_017009972.1:c.12045C>T	XP_016865461.1:p.Ala4015=
XM_017009973.1:c.12024C>T	XP_016865462.1:p.Ala4008=
XR_001742795.1:n.225-11697G>A
XR_001742796.1:n.225-27891G>A
XR_001742797.1:n.225-2581G>A