Canonical Allele Identifier: CA360425673
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823544G>C , CM000667.2:g.90823544G>C GRCh38
NC_000005.9:g.90119361G>C , CM000667.1:g.90119361G>C GRCh37
NC_000005.8:g.90155117G>C NCBI36
NG_007083.1:g.269745G>C
NG_007083.2:g.299201G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16316G>C MANE Select ENSP00000384582.2:p.Cys5439Ser
ENST00000425867.3:c.5270G>C ENSP00000392618.3:p.Cys1757Ser
ENST00000638510.1:n.3583G>C
ENST00000639431.1:c.265+147335G>C ENSP00000491057.1:n.265+147335G>C
ENST00000640061.1:n.128+1362G>C
ENST00000640407.1:c.2726G>C ENSP00000491425.1:p.Cys909Ser
ENST00000405460.6:c.16316G>C ENSP00000384582.2:p.Cys5439Ser
ENST00000425867.2:c.3299G>C ENSP00000392618.2:p.Cys1100Ser
NM_032119.3:c.16316G>C NP_115495.3:p.Cys5439Ser
NR_003149.1:n.16329G>C
XM_011543675.1:c.16313G>C XP_011541977.1:p.Cys5438Ser
XM_011543676.1:c.16235G>C XP_011541978.1:p.Cys5412Ser
XM_011543677.1:c.13619G>C XP_011541979.1:p.Cys4540Ser
NM_032119.4:c.16316G>C MANE Select NP_115495.3:p.Cys5439Ser
XM_017009963.2:c.16337G>C XP_016865452.1:p.Cys5446Ser
XM_017009964.2:c.16334G>C XP_016865453.1:p.Cys5445Ser
XM_017009965.1:c.16334G>C XP_016865454.1:p.Cys5445Ser
XM_017009966.2:c.16256G>C XP_016865455.1:p.Cys5419Ser
XM_017009967.1:c.16241G>C XP_016865456.1:p.Cys5414Ser
XM_017009968.2:c.16157G>C XP_016865457.1:p.Cys5386Ser
XM_017009969.2:c.16337G>C XP_016865458.1:p.Cys5446Ser
XM_017009972.1:c.9455G>C XP_016865461.1:p.Cys3152Ser
XM_017009973.1:c.9434G>C XP_016865462.1:p.Cys3145Ser
NR_003149.2:n.16332G>C