Canonical Allele Identifier: CA2709407590
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs1449260579

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823779T>A , CM000667.2:g.90823779T>A GRCh38
NC_000005.9:g.90119596T>A , CM000667.1:g.90119596T>A GRCh37
NC_000005.8:g.90155352T>A NCBI36
NG_007083.1:g.269980T>A
NG_007083.2:g.299436T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16368+183T>A MANE Select ENSP00000384582.2:n.16368+183T>A
ENST00000425867.3:c.5322+183T>A ENSP00000392618.3:n.5322+183T>A
ENST00000638510.1:n.3635+183T>A
ENST00000639431.1:c.265+147570T>A ENSP00000491057.1:n.265+147570T>A
ENST00000640061.1:n.128+1597T>A
ENST00000640407.1:c.2778+183T>A ENSP00000491425.1:n.2778+183T>A
ENST00000405460.6:c.16368+183T>A ENSP00000384582.2:n.16368+183T>A
ENST00000425867.2:c.3351+183T>A ENSP00000392618.2:n.3351+183T>A
NM_032119.3:c.16368+183T>A NP_115495.3:n.16368+183T>A
NR_003149.1:n.16381+183T>A
XM_011543675.1:c.16365+183T>A XP_011541977.1:n.16365+183T>A
XM_011543676.1:c.16287+183T>A XP_011541978.1:n.16287+183T>A
XM_011543677.1:c.13671+183T>A XP_011541979.1:n.13671+183T>A
NM_032119.4:c.16368+183T>A MANE Select NP_115495.3:n.16368+183T>A
XM_017009963.2:c.16389+183T>A XP_016865452.1:n.16389+183T>A
XM_017009964.2:c.16386+183T>A XP_016865453.1:n.16386+183T>A
XM_017009965.1:c.16386+183T>A XP_016865454.1:n.16386+183T>A
XM_017009966.2:c.16308+183T>A XP_016865455.1:n.16308+183T>A
XM_017009967.1:c.16293+183T>A XP_016865456.1:n.16293+183T>A
XM_017009968.2:c.16209+183T>A XP_016865457.1:n.16209+183T>A
XM_017009969.2:c.16389+183T>A XP_016865458.1:n.16389+183T>A
XM_017009972.1:c.9507+183T>A XP_016865461.1:n.9507+183T>A
XM_017009973.1:c.9486+183T>A XP_016865462.1:n.9486+183T>A
NR_003149.2:n.16384+183T>A