Canonical Allele Identifier: CA354222180

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003582A>T (hg19) ; chr3:g.123284735A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284735A>T , CM000665.2:g.123284735A>T	GRCh38
NC_000003.11:g.123003582A>T , CM000665.1:g.123003582A>T	GRCh37
NC_000003.10:g.124486272A>T	NCBI36
NG_033882.1:g.168811T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2336T>A	ENSP00000420082.2:p.Val779Asp
ENST00000470367.2:c.2624T>A	ENSP00000514541.1:p.Val875Asp
ENST00000483566.2:c.2336T>A	ENSP00000420252.2:p.Val779Asp
ENST00000699714.1:c.2336T>A	ENSP00000514539.1:p.Val779Asp
ENST00000699715.1:c.2336T>A	ENSP00000514540.1:p.Val779Asp
ENST00000699716.1:c.2336T>A	ENSP00000514542.1:p.Val779Asp
ENST00000699717.1:n.2062T>A
ENST00000699718.1:c.3734T>A	ENSP00000514543.1:p.Val1245Asp
ENST00000462833.6:c.3659T>A MANE Select	ENSP00000419361.1:p.Val1220Asp
ENST00000309879.9:c.2609T>A	ENSP00000308685.5:p.Val870Asp
ENST00000462833.5:c.3659T>A	ENSP00000419361.1:p.Val1220Asp
ENST00000478092.1:n.429T>A
ENST00000491190.5:c.2633T>A	ENSP00000418537.1:p.Val878Asp
NM_001199642.1:c.2609T>A	NP_001186571.1:p.Val870Asp
NM_183357.2:c.3659T>A	NP_899200.1:p.Val1220Asp
XM_005247077.2:c.3734T>A	XP_005247134.1:p.Val1245Asp
XM_005247078.1:c.2684T>A	XP_005247135.1:p.Val895Asp
XM_006713483.1:c.2633T>A	XP_006713546.1:p.Val878Asp
XM_006713484.1:c.2411T>A	XP_006713547.1:p.Val804Asp
XM_011512359.1:c.2735T>A	XP_011510661.1:p.Val912Asp
XM_011512360.1:c.2645T>A	XP_011510662.1:p.Val882Asp
XM_011512361.1:c.2411T>A	XP_011510663.1:p.Val804Asp
XM_005247077.4:c.3734T>A	XP_005247134.1:p.Val1245Asp
XM_011512359.2:c.2735T>A	XP_011510661.1:p.Val912Asp
XM_011512360.3:c.2645T>A	XP_011510662.1:p.Val882Asp
XM_017005638.1:c.2636T>A	XP_016861127.1:p.Val879Asp
XM_017005639.1:c.2636T>A	XP_016861128.1:p.Val879Asp
NM_001378259.1:c.3734T>A	NP_001365188.1:p.Val1245Asp
NM_183357.3:c.3659T>A MANE Select	NP_899200.1:p.Val1220Asp