Canonical Allele Identifier: CA2838325551
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617927dup , CM000667.2:g.90617927dup GRCh38
NC_000005.9:g.89913744dup , CM000667.1:g.89913744dup GRCh37
NC_000005.8:g.89949500dup NCBI36
NG_007083.1:g.64128dup
NG_007083.2:g.93584dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.331dup MANE Select ENSP00000384582.2:p.Thr111AsnfsTer?
ENST00000638316.1:n.541dup
ENST00000638638.1:n.738dup
ENST00000640083.1:n.36dup
ENST00000640109.1:n.427dup
ENST00000640281.1:n.390dup
ENST00000405460.6:c.331dup ENSP00000384582.2:p.Thr111AsnfsTer?
ENST00000508842.5:c.343dup ENSP00000425936.1:p.Thr115AsnfsTer17
NM_032119.3:c.331dup NP_115495.3:p.Thr111AsnfsTer?
NR_003149.1:n.427dup
XM_011543675.1:c.331dup XP_011541977.1:p.Thr111AsnfsTer?
XM_011543676.1:c.331dup XP_011541978.1:p.Thr111AsnfsTer?
XM_011543678.1:c.331dup XP_011541980.1:p.Thr111AsnfsTer?
XM_011543679.1:c.331dup XP_011541981.1:p.Thr111AsnfsTer?
NM_032119.4:c.331dup MANE Select NP_115495.3:p.Thr111AsnfsTer?
XM_017009963.2:c.331dup XP_016865452.1:p.Thr111AsnfsTer?
XM_017009964.2:c.331dup XP_016865453.1:p.Thr111AsnfsTer?
XM_017009965.1:c.328dup XP_016865454.1:p.Thr110AsnfsTer?
XM_017009966.2:c.331dup XP_016865455.1:p.Thr111AsnfsTer?
XM_017009967.1:c.331dup XP_016865456.1:p.Thr111AsnfsTer17
XM_017009968.2:c.331dup XP_016865457.1:p.Thr111AsnfsTer?
XM_017009969.2:c.331dup XP_016865458.1:p.Thr111AsnfsTer?
XM_017009970.2:c.331dup XP_016865459.1:p.Thr111AsnfsTer?
XM_017009971.2:c.331dup XP_016865460.1:p.Thr111AsnfsTer?
XM_017009974.2:c.331dup XP_016865463.1:p.Thr111AsnfsTer?
NR_003149.2:n.430dup