Canonical Allele Identifier: CA360425739
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823573A>T , CM000667.2:g.90823573A>T GRCh38
NC_000005.9:g.90119390A>T , CM000667.1:g.90119390A>T GRCh37
NC_000005.8:g.90155146A>T NCBI36
NG_007083.1:g.269774A>T
NG_007083.2:g.299230A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16345A>T MANE Select ENSP00000384582.2:p.Ser5449Cys
ENST00000425867.3:c.5299A>T ENSP00000392618.3:p.Ser1767Cys
ENST00000638510.1:n.3612A>T
ENST00000639431.1:c.265+147364A>T ENSP00000491057.1:n.265+147364A>T
ENST00000640061.1:n.128+1391A>T
ENST00000640407.1:c.2755A>T ENSP00000491425.1:p.Ser919Cys
ENST00000405460.6:c.16345A>T ENSP00000384582.2:p.Ser5449Cys
ENST00000425867.2:c.3328A>T ENSP00000392618.2:p.Ser1110Cys
NM_032119.3:c.16345A>T NP_115495.3:p.Ser5449Cys
NR_003149.1:n.16358A>T
XM_011543675.1:c.16342A>T XP_011541977.1:p.Ser5448Cys
XM_011543676.1:c.16264A>T XP_011541978.1:p.Ser5422Cys
XM_011543677.1:c.13648A>T XP_011541979.1:p.Ser4550Cys
NM_032119.4:c.16345A>T MANE Select NP_115495.3:p.Ser5449Cys
XM_017009963.2:c.16366A>T XP_016865452.1:p.Ser5456Cys
XM_017009964.2:c.16363A>T XP_016865453.1:p.Ser5455Cys
XM_017009965.1:c.16363A>T XP_016865454.1:p.Ser5455Cys
XM_017009966.2:c.16285A>T XP_016865455.1:p.Ser5429Cys
XM_017009967.1:c.16270A>T XP_016865456.1:p.Ser5424Cys
XM_017009968.2:c.16186A>T XP_016865457.1:p.Ser5396Cys
XM_017009969.2:c.16366A>T XP_016865458.1:p.Ser5456Cys
XM_017009972.1:c.9484A>T XP_016865461.1:p.Ser3162Cys
XM_017009973.1:c.9463A>T XP_016865462.1:p.Ser3155Cys
NR_003149.2:n.16361A>T