Canonical Allele Identifier: CA2767424552

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823714_90823715insA , CM000667.2:g.90823714_90823715insA	GRCh38
NC_000005.9:g.90119531_90119532insA , CM000667.1:g.90119531_90119532insA	GRCh37
NC_000005.8:g.90155287_90155288insA	NCBI36
NG_007083.1:g.269915_269916insA
NG_007083.2:g.299371_299372insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16368+118_16368+119insA MANE Select	ENSP00000384582.2:n.16368+118_16368+119insA
ENST00000425867.3:c.5322+118_5322+119insA	ENSP00000392618.3:n.5322+118_5322+119insA
ENST00000638510.1:n.3635+118_3635+119insA
ENST00000639431.1:c.265+147505_265+147506insA	ENSP00000491057.1:n.265+147505_265+147506insA
ENST00000640061.1:n.128+1532_128+1533insA
ENST00000640407.1:c.2778+118_2778+119insA	ENSP00000491425.1:n.2778+118_2778+119insA
ENST00000405460.6:c.16368+118_16368+119insA	ENSP00000384582.2:n.16368+118_16368+119insA
ENST00000425867.2:c.3351+118_3351+119insA	ENSP00000392618.2:n.3351+118_3351+119insA
NM_032119.3:c.16368+118_16368+119insA	NP_115495.3:n.16368+118_16368+119insA
NR_003149.1:n.16381+118_16381+119insA
XM_011543675.1:c.16365+118_16365+119insA	XP_011541977.1:n.16365+118_16365+119insA
XM_011543676.1:c.16287+118_16287+119insA	XP_011541978.1:n.16287+118_16287+119insA
XM_011543677.1:c.13671+118_13671+119insA	XP_011541979.1:n.13671+118_13671+119insA
NM_032119.4:c.16368+118_16368+119insA MANE Select	NP_115495.3:n.16368+118_16368+119insA
XM_017009963.2:c.16389+118_16389+119insA	XP_016865452.1:n.16389+118_16389+119insA
XM_017009964.2:c.16386+118_16386+119insA	XP_016865453.1:n.16386+118_16386+119insA
XM_017009965.1:c.16386+118_16386+119insA	XP_016865454.1:n.16386+118_16386+119insA
XM_017009966.2:c.16308+118_16308+119insA	XP_016865455.1:n.16308+118_16308+119insA
XM_017009967.1:c.16293+118_16293+119insA	XP_016865456.1:n.16293+118_16293+119insA
XM_017009968.2:c.16209+118_16209+119insA	XP_016865457.1:n.16209+118_16209+119insA
XM_017009969.2:c.16389+118_16389+119insA	XP_016865458.1:n.16389+118_16389+119insA
XM_017009972.1:c.9507+118_9507+119insA	XP_016865461.1:n.9507+118_9507+119insA
XM_017009973.1:c.9486+118_9486+119insA	XP_016865462.1:n.9486+118_9486+119insA
NR_003149.2:n.16384+118_16384+119insA