Canonical Allele Identifier: CA360425466
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823437T>A , CM000667.2:g.90823437T>A GRCh38
NC_000005.9:g.90119254T>A , CM000667.1:g.90119254T>A GRCh37
NC_000005.8:g.90155010T>A NCBI36
NG_007083.1:g.269638T>A
NG_007083.2:g.299094T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16209T>A MANE Select ENSP00000384582.2:p.Asp5403Glu
ENST00000425867.3:c.5163T>A ENSP00000392618.3:p.Asp1721Glu
ENST00000638510.1:n.3476T>A
ENST00000639431.1:c.265+147228T>A ENSP00000491057.1:n.265+147228T>A
ENST00000640061.1:n.128+1255T>A
ENST00000640407.1:c.2619T>A ENSP00000491425.1:p.Asp873Glu
ENST00000405460.6:c.16209T>A ENSP00000384582.2:p.Asp5403Glu
ENST00000425867.2:c.3192T>A ENSP00000392618.2:p.Asp1064Glu
NM_032119.3:c.16209T>A NP_115495.3:p.Asp5403Glu
NR_003149.1:n.16222T>A
XM_011543675.1:c.16206T>A XP_011541977.1:p.Asp5402Glu
XM_011543676.1:c.16128T>A XP_011541978.1:p.Asp5376Glu
XM_011543677.1:c.13512T>A XP_011541979.1:p.Asp4504Glu
NM_032119.4:c.16209T>A MANE Select NP_115495.3:p.Asp5403Glu
XM_017009963.2:c.16230T>A XP_016865452.1:p.Asp5410Glu
XM_017009964.2:c.16227T>A XP_016865453.1:p.Asp5409Glu
XM_017009965.1:c.16227T>A XP_016865454.1:p.Asp5409Glu
XM_017009966.2:c.16149T>A XP_016865455.1:p.Asp5383Glu
XM_017009967.1:c.16134T>A XP_016865456.1:p.Asp5378Glu
XM_017009968.2:c.16050T>A XP_016865457.1:p.Asp5350Glu
XM_017009969.2:c.16230T>A XP_016865458.1:p.Asp5410Glu
XM_017009972.1:c.9348T>A XP_016865461.1:p.Asp3116Glu
XM_017009973.1:c.9327T>A XP_016865462.1:p.Asp3109Glu
NR_003149.2:n.16225T>A