Canonical Allele Identifier: CA2674578344

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823643-TTTAGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823647_90823652del , CM000667.2:g.90823647_90823652del	GRCh38
NC_000005.9:g.90119464_90119469del , CM000667.1:g.90119464_90119469del	GRCh37
NC_000005.8:g.90155220_90155225del	NCBI36
NG_007083.1:g.269848_269853del
NG_007083.2:g.299304_299309del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16368+51_16368+56del MANE Select	ENSP00000384582.2:n.16368+51_16368+56del
ENST00000425867.3:c.5322+51_5322+56del	ENSP00000392618.3:n.5322+51_5322+56del
ENST00000638510.1:n.3635+51_3635+56del
ENST00000639431.1:c.265+147438_265+147443del	ENSP00000491057.1:n.265+147438_265+147443del
ENST00000640061.1:n.128+1465_128+1470del
ENST00000640407.1:c.2778+51_2778+56del	ENSP00000491425.1:n.2778+51_2778+56del
ENST00000405460.6:c.16368+51_16368+56del	ENSP00000384582.2:n.16368+51_16368+56del
ENST00000425867.2:c.3351+51_3351+56del	ENSP00000392618.2:n.3351+51_3351+56del
NM_032119.3:c.16368+51_16368+56del	NP_115495.3:n.16368+51_16368+56del
NR_003149.1:n.16381+51_16381+56del
XM_011543675.1:c.16365+51_16365+56del	XP_011541977.1:n.16365+51_16365+56del
XM_011543676.1:c.16287+51_16287+56del	XP_011541978.1:n.16287+51_16287+56del
XM_011543677.1:c.13671+51_13671+56del	XP_011541979.1:n.13671+51_13671+56del
NM_032119.4:c.16368+51_16368+56del MANE Select	NP_115495.3:n.16368+51_16368+56del
XM_017009963.2:c.16389+51_16389+56del	XP_016865452.1:n.16389+51_16389+56del
XM_017009964.2:c.16386+51_16386+56del	XP_016865453.1:n.16386+51_16386+56del
XM_017009965.1:c.16386+51_16386+56del	XP_016865454.1:n.16386+51_16386+56del
XM_017009966.2:c.16308+51_16308+56del	XP_016865455.1:n.16308+51_16308+56del
XM_017009967.1:c.16293+51_16293+56del	XP_016865456.1:n.16293+51_16293+56del
XM_017009968.2:c.16209+51_16209+56del	XP_016865457.1:n.16209+51_16209+56del
XM_017009969.2:c.16389+51_16389+56del	XP_016865458.1:n.16389+51_16389+56del
XM_017009972.1:c.9507+51_9507+56del	XP_016865461.1:n.9507+51_9507+56del
XM_017009973.1:c.9486+51_9486+56del	XP_016865462.1:n.9486+51_9486+56del
NR_003149.2:n.16384+51_16384+56del