Canonical Allele Identifier: CA1819965908
Gene: ADCY8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130795978_130795979delinsTA , CM000670.2:g.130795978_130795979delinsTA GRCh38
NC_000008.10:g.131808224_131808225delinsTA , CM000670.1:g.131808224_131808225delinsTA GRCh37
NC_000008.9:g.131877406_131877407delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000286355.10:c.3060+4447_3060+4448delinsTA MANE Select ENSP00000286355.5:n.3060+4447_3060+4448de...
ENST00000286355.9:c.3060+4447_3060+4448delinsTA ENSP00000286355.5:n.3060+4447_3060+4448de...
ENST00000377928.7:c.2667+4447_2667+4448delinsTA ENSP00000367161.3:n.2667+4447_2667+4448de...
NM_001115.2:c.3060+4447_3060+4448delinsTA NP_001106.1:n.3060+4447_3060+4448delinsTA...
XM_005250769.2:c.2970+4447_2970+4448delinsTA XP_005250826.1:n.2970+4447_2970+4448delin...
XM_006716501.2:c.2862+4447_2862+4448delinsTA XP_006716564.1:n.2862+4447_2862+4448delin...
XM_005250769.3:c.2970+4447_2970+4448delinsTA XP_005250826.1:n.2970+4447_2970+4448delin...
XM_006716501.3:c.2862+4447_2862+4448delinsTA XP_006716564.1:n.2862+4447_2862+4448delin...
XM_017013006.1:c.2772+4447_2772+4448delinsTA XP_016868495.1:n.2772+4447_2772+4448delin...
NM_001115.3:c.3060+4447_3060+4448delinsTA MANE Select NP_001106.1:n.3060+4447_3060+4448delinsTA...