Canonical Allele Identifier: CA435431401

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123010089G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291242G>C , CM000665.2:g.123291242G>C	GRCh38
NC_000003.11:g.123010089G>C , CM000665.1:g.123010089G>C	GRCh37
NC_000003.10:g.124492779G>C	NCBI36
NG_033882.1:g.162304C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1875C>G	ENSP00000420082.2:p.Ser625=
ENST00000470367.2:c.2163C>G	ENSP00000514541.1:p.Ser721=
ENST00000483566.2:c.1875C>G	ENSP00000420252.2:p.Ser625=
ENST00000699714.1:c.1875C>G	ENSP00000514539.1:p.Ser625=
ENST00000699715.1:c.1875C>G	ENSP00000514540.1:p.Ser625=
ENST00000699716.1:c.1875C>G	ENSP00000514542.1:p.Ser625=
ENST00000699717.1:n.1601C>G
ENST00000699718.1:c.3273C>G	ENSP00000514543.1:p.Ser1091=
ENST00000462833.6:c.3198C>G MANE Select	ENSP00000419361.1:p.Ser1066=
ENST00000309879.9:c.2148C>G	ENSP00000308685.5:p.Ser716=
ENST00000462833.5:c.3198C>G	ENSP00000419361.1:p.Ser1066=
ENST00000491190.5:c.2172C>G	ENSP00000418537.1:p.Ser724=
NM_001199642.1:c.2148C>G	NP_001186571.1:p.Ser716=
NM_183357.2:c.3198C>G	NP_899200.1:p.Ser1066=
XM_005247077.2:c.3273C>G	XP_005247134.1:p.Ser1091=
XM_005247078.1:c.2223C>G	XP_005247135.1:p.Ser741=
XM_006713483.1:c.2172C>G	XP_006713546.1:p.Ser724=
XM_006713484.1:c.1950C>G	XP_006713547.1:p.Ser650=
XM_011512359.1:c.2274C>G	XP_011510661.1:p.Ser758=
XM_011512360.1:c.2184C>G	XP_011510662.1:p.Ser728=
XM_011512361.1:c.1950C>G	XP_011510663.1:p.Ser650=
XM_005247077.4:c.3273C>G	XP_005247134.1:p.Ser1091=
XM_011512359.2:c.2274C>G	XP_011510661.1:p.Ser758=
XM_011512360.3:c.2184C>G	XP_011510662.1:p.Ser728=
XM_017005638.1:c.2175C>G	XP_016861127.1:p.Ser725=
XM_017005639.1:c.2175C>G	XP_016861128.1:p.Ser725=
NM_001378259.1:c.3273C>G	NP_001365188.1:p.Ser1091=
NM_183357.3:c.3198C>G MANE Select	NP_899200.1:p.Ser1066=