Canonical Allele Identifier: CA4877648
Gene: ADCY8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130780614G>C , CM000670.2:g.130780614G>C GRCh38
NC_000008.10:g.131792860G>C , CM000670.1:g.131792860G>C GRCh37
NC_000008.9:g.131862042G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286355.10:c.3532C>G MANE Select ENSP00000286355.5:p.Pro1178Ala
ENST00000286355.9:c.3532C>G ENSP00000286355.5:p.Pro1178Ala
ENST00000377928.7:c.3139C>G ENSP00000367161.3:p.Pro1047Ala
NM_001115.2:c.3532C>G NP_001106.1:p.Pro1178Ala
XM_005250769.2:c.3442C>G XP_005250826.1:p.Pro1148Ala
XM_006716501.2:c.3334C>G XP_006716564.1:p.Pro1112Ala
XM_005250769.3:c.3442C>G XP_005250826.1:p.Pro1148Ala
XM_006716501.3:c.3334C>G XP_006716564.1:p.Pro1112Ala
XM_017013006.1:c.3244C>G XP_016868495.1:p.Pro1082Ala
NM_001115.3:c.3532C>G MANE Select NP_001106.1:p.Pro1178Ala