Canonical Allele Identifier: CA1398370068
Gene: ADCY5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.123377911G= , CM000665.2:g.123377911G= GRCh38
NC_000003.11:g.123096758G= , CM000665.1:g.123096758G= GRCh37
NC_000003.10:g.124579448G= NCBI36
NG_033882.1:g.75635C=

Transcript Alleles

HGVS Amino-acid change
ENST00000466617.6:c.-189-25330C= ENSP00000420082.2:n.-189-25330C=
ENST00000470367.2:c.100-25330C= ENSP00000514541.1:n.100-25330C=
ENST00000483566.2:c.-189-25330C= ENSP00000420252.2:n.-189-25330C=
ENST00000699714.1:c.-189-25330C= ENSP00000514539.1:n.-189-25330C=
ENST00000699715.1:c.-189-25330C= ENSP00000514540.1:n.-189-25330C=
ENST00000699716.1:c.-189-25330C= ENSP00000514542.1:n.-189-25330C=
ENST00000699718.1:c.1135-25330C= ENSP00000514543.1:n.1135-25330C=
ENST00000462833.6:c.1135-25330C= MANE Select ENSP00000419361.1:n.1135-25330C=
ENST00000309879.9:c.85-25330C= ENSP00000308685.5:n.85-25330C=
ENST00000462833.5:c.1135-25330C= ENSP00000419361.1:n.1135-25330C=
ENST00000466617.5:c.-189-25330C= ENSP00000420082.1:n.-189-25330C=
ENST00000470367.1:n.430-25330C=
ENST00000476455.1:c.-109-9865C= ENSP00000417789.1:n.-109-9865C=
ENST00000483566.1:c.-189-25330C= ENSP00000420252.1:n.-189-25330C=
ENST00000491190.5:c.-109-9865C= ENSP00000418537.1:n.-109-9865C=
NM_001199642.1:c.85-25330C= NP_001186571.1:n.85-25330C=
NM_183357.2:c.1135-25330C= NP_899200.1:n.1135-25330C=
XM_005247077.2:c.1135-25330C= XP_005247134.1:n.1135-25330C=
XM_005247078.1:c.85-25330C= XP_005247135.1:n.85-25330C=
XM_006713484.1:c.-189-25330C= XP_006713547.1:n.-189-25330C=
XM_011512358.1:c.1135-25330C= XP_011510660.1:n.1135-25330C=
XM_011512359.1:c.136-25330C= XP_011510661.1:n.136-25330C=
XM_011512361.1:c.-189-25330C= XP_011510663.1:n.-189-25330C=
XM_005247077.4:c.1135-25330C= XP_005247134.1:n.1135-25330C=
XM_011512359.2:c.136-25330C= XP_011510661.1:n.136-25330C=
XM_017005638.1:c.36+12430C= XP_016861127.1:n.36+12430C=
XM_017005639.1:c.36+12884C= XP_016861128.1:n.36+12884C=
NM_001378259.1:c.1135-25330C= NP_001365188.1:n.1135-25330C=
NM_183357.3:c.1135-25330C= MANE Select NP_899200.1:n.1135-25330C=