Canonical Allele Identifier: CA354223728

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123010147T>A (hg19) ; chr3:g.123291300T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291300T>A , CM000665.2:g.123291300T>A	GRCh38
NC_000003.11:g.123010147T>A , CM000665.1:g.123010147T>A	GRCh37
NC_000003.10:g.124492837T>A	NCBI36
NG_033882.1:g.162246A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1817A>T	ENSP00000420082.2:p.Asp606Val
ENST00000470367.2:c.2105A>T	ENSP00000514541.1:p.Asp702Val
ENST00000483566.2:c.1817A>T	ENSP00000420252.2:p.Asp606Val
ENST00000699714.1:c.1817A>T	ENSP00000514539.1:p.Asp606Val
ENST00000699715.1:c.1817A>T	ENSP00000514540.1:p.Asp606Val
ENST00000699716.1:c.1817A>T	ENSP00000514542.1:p.Asp606Val
ENST00000699717.1:n.1543A>T
ENST00000699718.1:c.3215A>T	ENSP00000514543.1:p.Asp1072Val
ENST00000462833.6:c.3140A>T MANE Select	ENSP00000419361.1:p.Asp1047Val
ENST00000309879.9:c.2090A>T	ENSP00000308685.5:p.Asp697Val
ENST00000462833.5:c.3140A>T	ENSP00000419361.1:p.Asp1047Val
ENST00000491190.5:c.2114A>T	ENSP00000418537.1:p.Asp705Val
NM_001199642.1:c.2090A>T	NP_001186571.1:p.Asp697Val
NM_183357.2:c.3140A>T	NP_899200.1:p.Asp1047Val
XM_005247077.2:c.3215A>T	XP_005247134.1:p.Asp1072Val
XM_005247078.1:c.2165A>T	XP_005247135.1:p.Asp722Val
XM_006713483.1:c.2114A>T	XP_006713546.1:p.Asp705Val
XM_006713484.1:c.1892A>T	XP_006713547.1:p.Asp631Val
XM_011512359.1:c.2216A>T	XP_011510661.1:p.Asp739Val
XM_011512360.1:c.2126A>T	XP_011510662.1:p.Asp709Val
XM_011512361.1:c.1892A>T	XP_011510663.1:p.Asp631Val
XM_005247077.4:c.3215A>T	XP_005247134.1:p.Asp1072Val
XM_011512359.2:c.2216A>T	XP_011510661.1:p.Asp739Val
XM_011512360.3:c.2126A>T	XP_011510662.1:p.Asp709Val
XM_017005638.1:c.2117A>T	XP_016861127.1:p.Asp706Val
XM_017005639.1:c.2117A>T	XP_016861128.1:p.Asp706Val
NM_001378259.1:c.3215A>T	NP_001365188.1:p.Asp1072Val
NM_183357.3:c.3140A>T MANE Select	NP_899200.1:p.Asp1047Val