Canonical Allele Identifier: CA435431376

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123010221G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291374G>C , CM000665.2:g.123291374G>C	GRCh38
NC_000003.11:g.123010221G>C , CM000665.1:g.123010221G>C	GRCh37
NC_000003.10:g.124492911G>C	NCBI36
NG_033882.1:g.162172C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1743C>G	ENSP00000420082.2:p.Ala581=
ENST00000470367.2:c.2031C>G	ENSP00000514541.1:p.Ala677=
ENST00000483566.2:c.1743C>G	ENSP00000420252.2:p.Ala581=
ENST00000699714.1:c.1743C>G	ENSP00000514539.1:p.Ala581=
ENST00000699715.1:c.1743C>G	ENSP00000514540.1:p.Ala581=
ENST00000699716.1:c.1743C>G	ENSP00000514542.1:p.Ala581=
ENST00000699717.1:n.1469C>G
ENST00000699718.1:c.3141C>G	ENSP00000514543.1:p.Ala1047=
ENST00000462833.6:c.3066C>G MANE Select	ENSP00000419361.1:p.Ala1022=
ENST00000309879.9:c.2016C>G	ENSP00000308685.5:p.Ala672=
ENST00000462833.5:c.3066C>G	ENSP00000419361.1:p.Ala1022=
ENST00000491190.5:c.2040C>G	ENSP00000418537.1:p.Ala680=
NM_001199642.1:c.2016C>G	NP_001186571.1:p.Ala672=
NM_183357.2:c.3066C>G	NP_899200.1:p.Ala1022=
XM_005247077.2:c.3141C>G	XP_005247134.1:p.Ala1047=
XM_005247078.1:c.2091C>G	XP_005247135.1:p.Ala697=
XM_006713483.1:c.2040C>G	XP_006713546.1:p.Ala680=
XM_006713484.1:c.1818C>G	XP_006713547.1:p.Ala606=
XM_011512359.1:c.2142C>G	XP_011510661.1:p.Ala714=
XM_011512360.1:c.2052C>G	XP_011510662.1:p.Ala684=
XM_011512361.1:c.1818C>G	XP_011510663.1:p.Ala606=
XM_005247077.4:c.3141C>G	XP_005247134.1:p.Ala1047=
XM_011512359.2:c.2142C>G	XP_011510661.1:p.Ala714=
XM_011512360.3:c.2052C>G	XP_011510662.1:p.Ala684=
XM_017005638.1:c.2043C>G	XP_016861127.1:p.Ala681=
XM_017005639.1:c.2043C>G	XP_016861128.1:p.Ala681=
NM_001378259.1:c.3141C>G	NP_001365188.1:p.Ala1047=
NM_183357.3:c.3066C>G MANE Select	NP_899200.1:p.Ala1022=