Canonical Allele Identifier: CA1562918327
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90823594A= , CM000667.2:g.90823594A= GRCh38
NC_000005.9:g.90119411A= , CM000667.1:g.90119411A= GRCh37
NC_000005.8:g.90155167A= NCBI36
NG_007083.1:g.269795A=
NG_007083.2:g.299251A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.16366A= MANE Select ENSP00000384582.2:p.Lys5456=
ENST00000425867.3:c.5320A= ENSP00000392618.3:p.Lys1774=
ENST00000638510.1:n.3633A=
ENST00000639431.1:c.265+147385A= ENSP00000491057.1:n.265+147385A=
ENST00000640061.1:n.128+1412A=
ENST00000640407.1:c.2776A= ENSP00000491425.1:p.Lys926=
ENST00000405460.6:c.16366A= ENSP00000384582.2:p.Lys5456=
ENST00000425867.2:c.3349A= ENSP00000392618.2:p.Lys1117=
NM_032119.3:c.16366A= NP_115495.3:p.Lys5456=
NR_003149.1:n.16379A=
XM_011543675.1:c.16363A= XP_011541977.1:p.Lys5455=
XM_011543676.1:c.16285A= XP_011541978.1:p.Lys5429=
XM_011543677.1:c.13669A= XP_011541979.1:p.Lys4557=
NM_032119.4:c.16366A= MANE Select NP_115495.3:p.Lys5456=
XM_017009963.2:c.16387A= XP_016865452.1:p.Lys5463=
XM_017009964.2:c.16384A= XP_016865453.1:p.Lys5462=
XM_017009965.1:c.16384A= XP_016865454.1:p.Lys5462=
XM_017009966.2:c.16306A= XP_016865455.1:p.Lys5436=
XM_017009967.1:c.16291A= XP_016865456.1:p.Lys5431=
XM_017009968.2:c.16207A= XP_016865457.1:p.Lys5403=
XM_017009969.2:c.16387A= XP_016865458.1:p.Lys5463=
XM_017009972.1:c.9505A= XP_016865461.1:p.Lys3169=
XM_017009973.1:c.9484A= XP_016865462.1:p.Lys3162=
NR_003149.2:n.16382A=