Canonical Allele Identifier: CA435431292

Gene: ADCY5

Linked Data

• dbSNP Id: rs774740790
• MyVariant Identifiers: chr3:g.123009975G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291128G>T , CM000665.2:g.123291128G>T	GRCh38
NC_000003.11:g.123009975G>T , CM000665.1:g.123009975G>T	GRCh37
NC_000003.10:g.124492665G>T	NCBI36
NG_033882.1:g.162418C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1989C>A	ENSP00000420082.2:p.Ile663=
ENST00000470367.2:c.2277C>A	ENSP00000514541.1:p.Ile759=
ENST00000483566.2:c.1989C>A	ENSP00000420252.2:p.Ile663=
ENST00000699714.1:c.1989C>A	ENSP00000514539.1:p.Ile663=
ENST00000699715.1:c.1989C>A	ENSP00000514540.1:p.Ile663=
ENST00000699716.1:c.1989C>A	ENSP00000514542.1:p.Ile663=
ENST00000699717.1:n.1715C>A
ENST00000699718.1:c.3387C>A	ENSP00000514543.1:p.Ile1129=
ENST00000462833.6:c.3312C>A MANE Select	ENSP00000419361.1:p.Ile1104=
ENST00000309879.9:c.2262C>A	ENSP00000308685.5:p.Ile754=
ENST00000462833.5:c.3312C>A	ENSP00000419361.1:p.Ile1104=
ENST00000491190.5:c.2286C>A	ENSP00000418537.1:p.Ile762=
NM_001199642.1:c.2262C>A	NP_001186571.1:p.Ile754=
NM_183357.2:c.3312C>A	NP_899200.1:p.Ile1104=
XM_005247077.2:c.3387C>A	XP_005247134.1:p.Ile1129=
XM_005247078.1:c.2337C>A	XP_005247135.1:p.Ile779=
XM_006713483.1:c.2286C>A	XP_006713546.1:p.Ile762=
XM_006713484.1:c.2064C>A	XP_006713547.1:p.Ile688=
XM_011512359.1:c.2388C>A	XP_011510661.1:p.Ile796=
XM_011512360.1:c.2298C>A	XP_011510662.1:p.Ile766=
XM_011512361.1:c.2064C>A	XP_011510663.1:p.Ile688=
XM_005247077.4:c.3387C>A	XP_005247134.1:p.Ile1129=
XM_011512359.2:c.2388C>A	XP_011510661.1:p.Ile796=
XM_011512360.3:c.2298C>A	XP_011510662.1:p.Ile766=
XM_017005638.1:c.2289C>A	XP_016861127.1:p.Ile763=
XM_017005639.1:c.2289C>A	XP_016861128.1:p.Ile763=
NM_001378259.1:c.3387C>A	NP_001365188.1:p.Ile1129=
NM_183357.3:c.3312C>A MANE Select	NP_899200.1:p.Ile1104=