Canonical Allele Identifier: CA3342758

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91163810A>G , CM000667.2:g.91163810A>G	GRCh38
NC_000005.9:g.90459627A>G , CM000667.1:g.90459627A>G	GRCh37
NC_000005.8:g.90495383A>G	NCBI36
NG_007083.1:g.610011A>G
NG_007083.2:g.639467A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18831A>G MANE Select	NP_115495.3:p.Glu6277=
ENST00000405460.9:c.18831A>G MANE Select	ENSP00000384582.2:p.Glu6277=
NM_032119.3:c.18831A>G	NP_115495.3:p.Glu6277=
NR_003149.1:n.18844A>G
NR_003149.2:n.18847A>G
ENST00000405460.6:c.18831A>G	ENSP00000384582.2:p.Glu6277=
ENST00000425867.2:c.5814A>G	ENSP00000392618.2:p.Glu1938=
ENST00000425867.3:c.7785A>G	ENSP00000392618.3:p.Glu2595=
ENST00000638510.1:n.6098A>G
ENST00000638990.1:c.2043A>G
ENST00000639212.1:n.751A>G
ENST00000639530.1:n.699A>G
ENST00000639821.1:c.545A>G	ENSP00000492216.1:p.Asn182Ser
ENST00000640256.1:n.507A>G
ENST00000640407.1:c.5280A>G	ENSP00000491425.1:n.5280A>G
ENST00000640815.1:c.915A>G	ENSP00000491767.1:p.Glu305=
XM_011543675.1:c.18828A>G	XP_011541977.1:p.Glu6276=
XM_011543676.1:c.18750A>G	XP_011541978.1:p.Glu6250=
XM_011543677.1:c.16134A>G	XP_011541979.1:p.Glu5378=
XM_017009963.2:c.18852A>G	XP_016865452.1:p.Glu6284=
XM_017009964.2:c.18849A>G	XP_016865453.1:p.Glu6283=
XM_017009965.1:c.18849A>G	XP_016865454.1:p.Glu6283=
XM_017009966.2:c.18771A>G	XP_016865455.1:p.Glu6257=
XM_017009967.1:c.18756A>G	XP_016865456.1:p.Glu6252=
XM_017009968.2:c.18672A>G	XP_016865457.1:p.Glu6224=
XM_017009969.2:c.18482A>G	XP_016865458.1:p.Asn6161Ser
XM_017009972.1:c.11970A>G	XP_016865461.1:p.Glu3990=
XM_017009973.1:c.11949A>G	XP_016865462.1:p.Glu3983=
XR_001742795.1:n.225-11622T>C
XR_001742796.1:n.225-27816T>C
XR_001742797.1:n.225-2506T>C