Canonical Allele Identifier: CA360425744
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823575C>A , CM000667.2:g.90823575C>A GRCh38
NC_000005.9:g.90119392C>A , CM000667.1:g.90119392C>A GRCh37
NC_000005.8:g.90155148C>A NCBI36
NG_007083.1:g.269776C>A
NG_007083.2:g.299232C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16347C>A MANE Select ENSP00000384582.2:p.Ser5449Arg
ENST00000425867.3:c.5301C>A ENSP00000392618.3:p.Ser1767Arg
ENST00000638510.1:n.3614C>A
ENST00000639431.1:c.265+147366C>A ENSP00000491057.1:n.265+147366C>A
ENST00000640061.1:n.128+1393C>A
ENST00000640407.1:c.2757C>A ENSP00000491425.1:p.Ser919Arg
ENST00000405460.6:c.16347C>A ENSP00000384582.2:p.Ser5449Arg
ENST00000425867.2:c.3330C>A ENSP00000392618.2:p.Ser1110Arg
NM_032119.3:c.16347C>A NP_115495.3:p.Ser5449Arg
NR_003149.1:n.16360C>A
XM_011543675.1:c.16344C>A XP_011541977.1:p.Ser5448Arg
XM_011543676.1:c.16266C>A XP_011541978.1:p.Ser5422Arg
XM_011543677.1:c.13650C>A XP_011541979.1:p.Ser4550Arg
NM_032119.4:c.16347C>A MANE Select NP_115495.3:p.Ser5449Arg
XM_017009963.2:c.16368C>A XP_016865452.1:p.Ser5456Arg
XM_017009964.2:c.16365C>A XP_016865453.1:p.Ser5455Arg
XM_017009965.1:c.16365C>A XP_016865454.1:p.Ser5455Arg
XM_017009966.2:c.16287C>A XP_016865455.1:p.Ser5429Arg
XM_017009967.1:c.16272C>A XP_016865456.1:p.Ser5424Arg
XM_017009968.2:c.16188C>A XP_016865457.1:p.Ser5396Arg
XM_017009969.2:c.16368C>A XP_016865458.1:p.Ser5456Arg
XM_017009972.1:c.9486C>A XP_016865461.1:p.Ser3162Arg
XM_017009973.1:c.9465C>A XP_016865462.1:p.Ser3155Arg
NR_003149.2:n.16363C>A