Canonical Allele Identifier: CA2767424533

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823657_90823658insAGC , CM000667.2:g.90823657_90823658insAGC	GRCh38
NC_000005.9:g.90119474_90119475insAGC , CM000667.1:g.90119474_90119475insAGC	GRCh37
NC_000005.8:g.90155230_90155231insAGC	NCBI36
NG_007083.1:g.269858_269859insAGC
NG_007083.2:g.299314_299315insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16368+61_16368+62insAGC MANE Select	ENSP00000384582.2:n.16368+61_16368+62insAGC
ENST00000425867.3:c.5322+61_5322+62insAGC	ENSP00000392618.3:n.5322+61_5322+62insAGC
ENST00000638510.1:n.3635+61_3635+62insAGC
ENST00000639431.1:c.265+147448_265+147449insAGC	ENSP00000491057.1:n.265+147448_265+147449insAGC
ENST00000640061.1:n.128+1475_128+1476insAGC
ENST00000640407.1:c.2778+61_2778+62insAGC	ENSP00000491425.1:n.2778+61_2778+62insAGC
ENST00000405460.6:c.16368+61_16368+62insAGC	ENSP00000384582.2:n.16368+61_16368+62insAGC
ENST00000425867.2:c.3351+61_3351+62insAGC	ENSP00000392618.2:n.3351+61_3351+62insAGC
NM_032119.3:c.16368+61_16368+62insAGC	NP_115495.3:n.16368+61_16368+62insAGC
NR_003149.1:n.16381+61_16381+62insAGC
XM_011543675.1:c.16365+61_16365+62insAGC	XP_011541977.1:n.16365+61_16365+62insAGC
XM_011543676.1:c.16287+61_16287+62insAGC	XP_011541978.1:n.16287+61_16287+62insAGC
XM_011543677.1:c.13671+61_13671+62insAGC	XP_011541979.1:n.13671+61_13671+62insAGC
NM_032119.4:c.16368+61_16368+62insAGC MANE Select	NP_115495.3:n.16368+61_16368+62insAGC
XM_017009963.2:c.16389+61_16389+62insAGC	XP_016865452.1:n.16389+61_16389+62insAGC
XM_017009964.2:c.16386+61_16386+62insAGC	XP_016865453.1:n.16386+61_16386+62insAGC
XM_017009965.1:c.16386+61_16386+62insAGC	XP_016865454.1:n.16386+61_16386+62insAGC
XM_017009966.2:c.16308+61_16308+62insAGC	XP_016865455.1:n.16308+61_16308+62insAGC
XM_017009967.1:c.16293+61_16293+62insAGC	XP_016865456.1:n.16293+61_16293+62insAGC
XM_017009968.2:c.16209+61_16209+62insAGC	XP_016865457.1:n.16209+61_16209+62insAGC
XM_017009969.2:c.16389+61_16389+62insAGC	XP_016865458.1:n.16389+61_16389+62insAGC
XM_017009972.1:c.9507+61_9507+62insAGC	XP_016865461.1:n.9507+61_9507+62insAGC
XM_017009973.1:c.9486+61_9486+62insAGC	XP_016865462.1:n.9486+61_9486+62insAGC
NR_003149.2:n.16384+61_16384+62insAGC