Canonical Allele Identifier: CA1398330487
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123291438_123291444delinsACCTCCT , CM000665.2:g.123291438_123291444delinsACCTCCT GRCh38
NC_000003.11:g.123010285_123010291delinsACCTCCT , CM000665.1:g.123010285_123010291delinsACCTCCT GRCh37
NC_000003.10:g.124492975_124492981delinsACCTCCT NCBI36
NG_033882.1:g.162102_162108delinsAGGAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000466617.6:c.1741-68_1741-62delinsAGGAGGT ENSP00000420082.2:n.1741-68_1741-62delinsAGGAGGT
ENST00000470367.2:c.2029-68_2029-62delinsAGGAGGT ENSP00000514541.1:n.2029-68_2029-62delinsAGGAGGT
ENST00000483566.2:c.1741-68_1741-62delinsAGGAGGT ENSP00000420252.2:n.1741-68_1741-62delinsAGGAGGT
ENST00000699714.1:c.1741-68_1741-62delinsAGGAGGT ENSP00000514539.1:n.1741-68_1741-62delinsAGGAGGT
ENST00000699715.1:c.1741-68_1741-62delinsAGGAGGT ENSP00000514540.1:n.1741-68_1741-62delinsAGGAGGT
ENST00000699716.1:c.1741-68_1741-62delinsAGGAGGT ENSP00000514542.1:n.1741-68_1741-62delinsAGGAGGT
ENST00000699717.1:n.1467-68_1467-62delinsAGGAGGT
ENST00000699718.1:c.3139-68_3139-62delinsAGGAGGT ENSP00000514543.1:n.3139-68_3139-62delinsAGGAGGT
ENST00000462833.6:c.3064-68_3064-62delinsAGGAGGT MANE Select ENSP00000419361.1:n.3064-68_3064-62delinsAGGAGGT
ENST00000309879.9:c.2014-68_2014-62delinsAGGAGGT ENSP00000308685.5:n.2014-68_2014-62delinsAGGAGGT
ENST00000462833.5:c.3064-68_3064-62delinsAGGAGGT ENSP00000419361.1:n.3064-68_3064-62delinsAGGAGGT
ENST00000491190.5:c.2038-68_2038-62delinsAGGAGGT ENSP00000418537.1:n.2038-68_2038-62delinsAGGAGGT
NM_001199642.1:c.2014-68_2014-62delinsAGGAGGT NP_001186571.1:n.2014-68_2014-62delinsAGGAGGT
NM_183357.2:c.3064-68_3064-62delinsAGGAGGT NP_899200.1:n.3064-68_3064-62delinsAGGAGGT
XM_005247077.2:c.3139-68_3139-62delinsAGGAGGT XP_005247134.1:n.3139-68_3139-62delinsAGGAGGT
XM_005247078.1:c.2089-68_2089-62delinsAGGAGGT XP_005247135.1:n.2089-68_2089-62delinsAGGAGGT
XM_006713483.1:c.2038-68_2038-62delinsAGGAGGT XP_006713546.1:n.2038-68_2038-62delinsAGGAGGT
XM_006713484.1:c.1816-68_1816-62delinsAGGAGGT XP_006713547.1:n.1816-68_1816-62delinsAGGAGGT
XM_011512359.1:c.2140-68_2140-62delinsAGGAGGT XP_011510661.1:n.2140-68_2140-62delinsAGGAGGT
XM_011512360.1:c.2050-68_2050-62delinsAGGAGGT XP_011510662.1:n.2050-68_2050-62delinsAGGAGGT
XM_011512361.1:c.1816-68_1816-62delinsAGGAGGT XP_011510663.1:n.1816-68_1816-62delinsAGGAGGT
XM_005247077.4:c.3139-68_3139-62delinsAGGAGGT XP_005247134.1:n.3139-68_3139-62delinsAGGAGGT
XM_011512359.2:c.2140-68_2140-62delinsAGGAGGT XP_011510661.1:n.2140-68_2140-62delinsAGGAGGT
XM_011512360.3:c.2050-68_2050-62delinsAGGAGGT XP_011510662.1:n.2050-68_2050-62delinsAGGAGGT
XM_017005638.1:c.2041-68_2041-62delinsAGGAGGT XP_016861127.1:n.2041-68_2041-62delinsAGGAGGT
XM_017005639.1:c.2041-68_2041-62delinsAGGAGGT XP_016861128.1:n.2041-68_2041-62delinsAGGAGGT
NM_001378259.1:c.3139-68_3139-62delinsAGGAGGT NP_001365188.1:n.3139-68_3139-62delinsAGGAGGT
NM_183357.3:c.3064-68_3064-62delinsAGGAGGT MANE Select NP_899200.1:n.3064-68_3064-62delinsAGGAGGT