Canonical Allele Identifier: CA4878431
Gene: ADCY8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.131039455G>C , CM000670.2:g.131039455G>C GRCh38
NC_000008.10:g.132051701G>C , CM000670.1:g.132051701G>C GRCh37
NC_000008.9:g.132120883G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286355.10:c.879C>G MANE Select ENSP00000286355.5:p.Ile293Met
ENST00000286355.9:c.879C>G ENSP00000286355.5:p.Ile293Met
ENST00000377928.7:c.879C>G ENSP00000367161.3:p.Ile293Met
NM_001115.2:c.879C>G NP_001106.1:p.Ile293Met
XM_005250769.2:c.879C>G XP_005250826.1:p.Ile293Met
XM_006716501.2:c.879C>G XP_006716564.1:p.Ile293Met
XM_005250769.3:c.879C>G XP_005250826.1:p.Ile293Met
XM_006716501.3:c.879C>G XP_006716564.1:p.Ile293Met
XM_017013006.1:c.879C>G XP_016868495.1:p.Ile293Met
XM_017013007.1:c.879C>G XP_016868496.1:p.Ile293Met
NM_001115.3:c.879C>G MANE Select NP_001106.1:p.Ile293Met