Canonical Allele Identifier: CA354223898

Gene: ADCY5

Linked Data

• dbSNP Id: rs1393206482
• gnomAD v3: 3-123291375-G-T
• gnomAD v4: 3-123291375-G-T
• MyVariant Identifiers: chr3:g.123010222G>T (hg19) ; chr3:g.123291375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291375G>T , CM000665.2:g.123291375G>T	GRCh38
NC_000003.11:g.123010222G>T , CM000665.1:g.123010222G>T	GRCh37
NC_000003.10:g.124492912G>T	NCBI36
NG_033882.1:g.162171C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1742C>A	ENSP00000420082.2:p.Ala581Asp
ENST00000470367.2:c.2030C>A	ENSP00000514541.1:p.Ala677Asp
ENST00000483566.2:c.1742C>A	ENSP00000420252.2:p.Ala581Asp
ENST00000699714.1:c.1742C>A	ENSP00000514539.1:p.Ala581Asp
ENST00000699715.1:c.1742C>A	ENSP00000514540.1:p.Ala581Asp
ENST00000699716.1:c.1742C>A	ENSP00000514542.1:p.Ala581Asp
ENST00000699717.1:n.1468C>A
ENST00000699718.1:c.3140C>A	ENSP00000514543.1:p.Ala1047Asp
ENST00000462833.6:c.3065C>A MANE Select	ENSP00000419361.1:p.Ala1022Asp
ENST00000309879.9:c.2015C>A	ENSP00000308685.5:p.Ala672Asp
ENST00000462833.5:c.3065C>A	ENSP00000419361.1:p.Ala1022Asp
ENST00000491190.5:c.2039C>A	ENSP00000418537.1:p.Ala680Asp
NM_001199642.1:c.2015C>A	NP_001186571.1:p.Ala672Asp
NM_183357.2:c.3065C>A	NP_899200.1:p.Ala1022Asp
XM_005247077.2:c.3140C>A	XP_005247134.1:p.Ala1047Asp
XM_005247078.1:c.2090C>A	XP_005247135.1:p.Ala697Asp
XM_006713483.1:c.2039C>A	XP_006713546.1:p.Ala680Asp
XM_006713484.1:c.1817C>A	XP_006713547.1:p.Ala606Asp
XM_011512359.1:c.2141C>A	XP_011510661.1:p.Ala714Asp
XM_011512360.1:c.2051C>A	XP_011510662.1:p.Ala684Asp
XM_011512361.1:c.1817C>A	XP_011510663.1:p.Ala606Asp
XM_005247077.4:c.3140C>A	XP_005247134.1:p.Ala1047Asp
XM_011512359.2:c.2141C>A	XP_011510661.1:p.Ala714Asp
XM_011512360.3:c.2051C>A	XP_011510662.1:p.Ala684Asp
XM_017005638.1:c.2042C>A	XP_016861127.1:p.Ala681Asp
XM_017005639.1:c.2042C>A	XP_016861128.1:p.Ala681Asp
NM_001378259.1:c.3140C>A	NP_001365188.1:p.Ala1047Asp
NM_183357.3:c.3065C>A MANE Select	NP_899200.1:p.Ala1022Asp