Canonical Allele Identifier: CA1819965866
Gene: ADCY8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130795906G= , CM000670.2:g.130795906G= GRCh38
NC_000008.10:g.131808152G= , CM000670.1:g.131808152G= GRCh37
NC_000008.9:g.131877334G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000286355.10:c.3060+4520C= MANE Select ENSP00000286355.5:n.3060+4520C=
ENST00000286355.9:c.3060+4520C= ENSP00000286355.5:n.3060+4520C=
ENST00000377928.7:c.2667+4520C= ENSP00000367161.3:n.2667+4520C=
NM_001115.2:c.3060+4520C= NP_001106.1:n.3060+4520C=
XM_005250769.2:c.2970+4520C= XP_005250826.1:n.2970+4520C=
XM_006716501.2:c.2862+4520C= XP_006716564.1:n.2862+4520C=
XM_005250769.3:c.2970+4520C= XP_005250826.1:n.2970+4520C=
XM_006716501.3:c.2862+4520C= XP_006716564.1:n.2862+4520C=
XM_017013006.1:c.2772+4520C= XP_016868495.1:n.2772+4520C=
NM_001115.3:c.3060+4520C= MANE Select NP_001106.1:n.3060+4520C=