Canonical Allele Identifier: CA2830538952
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823761_90823772del , CM000667.2:g.90823761_90823772del GRCh38
NC_000005.9:g.90119578_90119589del , CM000667.1:g.90119578_90119589del GRCh37
NC_000005.8:g.90155334_90155345del NCBI36
NG_007083.1:g.269962_269973del
NG_007083.2:g.299418_299429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16368+165_16368+176del MANE Select ENSP00000384582.2:n.16368+165_16368+176del
ENST00000425867.3:c.5322+165_5322+176del ENSP00000392618.3:n.5322+165_5322+176del
ENST00000638510.1:n.3635+165_3635+176del
ENST00000639431.1:c.265+147552_265+147563del ENSP00000491057.1:n.265+147552_265+147563del
ENST00000640061.1:n.128+1579_128+1590del
ENST00000640407.1:c.2778+165_2778+176del ENSP00000491425.1:n.2778+165_2778+176del
ENST00000405460.6:c.16368+165_16368+176del ENSP00000384582.2:n.16368+165_16368+176del
ENST00000425867.2:c.3351+165_3351+176del ENSP00000392618.2:n.3351+165_3351+176del
NM_032119.3:c.16368+165_16368+176del NP_115495.3:n.16368+165_16368+176del
NR_003149.1:n.16381+165_16381+176del
XM_011543675.1:c.16365+165_16365+176del XP_011541977.1:n.16365+165_16365+176del
XM_011543676.1:c.16287+165_16287+176del XP_011541978.1:n.16287+165_16287+176del
XM_011543677.1:c.13671+165_13671+176del XP_011541979.1:n.13671+165_13671+176del
NM_032119.4:c.16368+165_16368+176del MANE Select NP_115495.3:n.16368+165_16368+176del
XM_017009963.2:c.16389+165_16389+176del XP_016865452.1:n.16389+165_16389+176del
XM_017009964.2:c.16386+165_16386+176del XP_016865453.1:n.16386+165_16386+176del
XM_017009965.1:c.16386+165_16386+176del XP_016865454.1:n.16386+165_16386+176del
XM_017009966.2:c.16308+165_16308+176del XP_016865455.1:n.16308+165_16308+176del
XM_017009967.1:c.16293+165_16293+176del XP_016865456.1:n.16293+165_16293+176del
XM_017009968.2:c.16209+165_16209+176del XP_016865457.1:n.16209+165_16209+176del
XM_017009969.2:c.16389+165_16389+176del XP_016865458.1:n.16389+165_16389+176del
XM_017009972.1:c.9507+165_9507+176del XP_016865461.1:n.9507+165_9507+176del
XM_017009973.1:c.9486+165_9486+176del XP_016865462.1:n.9486+165_9486+176del
NR_003149.2:n.16384+165_16384+176del