Canonical Allele Identifier: CA354223555

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123010067A>T (hg19) ; chr3:g.123291220A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291220A>T , CM000665.2:g.123291220A>T	GRCh38
NC_000003.11:g.123010067A>T , CM000665.1:g.123010067A>T	GRCh37
NC_000003.10:g.124492757A>T	NCBI36
NG_033882.1:g.162326T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1897T>A	ENSP00000420082.2:p.Phe633Ile
ENST00000470367.2:c.2185T>A	ENSP00000514541.1:p.Phe729Ile
ENST00000483566.2:c.1897T>A	ENSP00000420252.2:p.Phe633Ile
ENST00000699714.1:c.1897T>A	ENSP00000514539.1:p.Phe633Ile
ENST00000699715.1:c.1897T>A	ENSP00000514540.1:p.Phe633Ile
ENST00000699716.1:c.1897T>A	ENSP00000514542.1:p.Phe633Ile
ENST00000699717.1:n.1623T>A
ENST00000699718.1:c.3295T>A	ENSP00000514543.1:p.Phe1099Ile
ENST00000462833.6:c.3220T>A MANE Select	ENSP00000419361.1:p.Phe1074Ile
ENST00000309879.9:c.2170T>A	ENSP00000308685.5:p.Phe724Ile
ENST00000462833.5:c.3220T>A	ENSP00000419361.1:p.Phe1074Ile
ENST00000491190.5:c.2194T>A	ENSP00000418537.1:p.Phe732Ile
NM_001199642.1:c.2170T>A	NP_001186571.1:p.Phe724Ile
NM_183357.2:c.3220T>A	NP_899200.1:p.Phe1074Ile
XM_005247077.2:c.3295T>A	XP_005247134.1:p.Phe1099Ile
XM_005247078.1:c.2245T>A	XP_005247135.1:p.Phe749Ile
XM_006713483.1:c.2194T>A	XP_006713546.1:p.Phe732Ile
XM_006713484.1:c.1972T>A	XP_006713547.1:p.Phe658Ile
XM_011512359.1:c.2296T>A	XP_011510661.1:p.Phe766Ile
XM_011512360.1:c.2206T>A	XP_011510662.1:p.Phe736Ile
XM_011512361.1:c.1972T>A	XP_011510663.1:p.Phe658Ile
XM_005247077.4:c.3295T>A	XP_005247134.1:p.Phe1099Ile
XM_011512359.2:c.2296T>A	XP_011510661.1:p.Phe766Ile
XM_011512360.3:c.2206T>A	XP_011510662.1:p.Phe736Ile
XM_017005638.1:c.2197T>A	XP_016861127.1:p.Phe733Ile
XM_017005639.1:c.2197T>A	XP_016861128.1:p.Phe733Ile
NM_001378259.1:c.3295T>A	NP_001365188.1:p.Phe1099Ile
NM_183357.3:c.3220T>A MANE Select	NP_899200.1:p.Phe1074Ile