Canonical Allele Identifier: CA354223404

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123010000C>A (hg19) ; chr3:g.123291153C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291153C>A , CM000665.2:g.123291153C>A	GRCh38
NC_000003.11:g.123010000C>A , CM000665.1:g.123010000C>A	GRCh37
NC_000003.10:g.124492690C>A	NCBI36
NG_033882.1:g.162393G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1964G>T	ENSP00000420082.2:p.Cys655Phe
ENST00000470367.2:c.2252G>T	ENSP00000514541.1:p.Cys751Phe
ENST00000483566.2:c.1964G>T	ENSP00000420252.2:p.Cys655Phe
ENST00000699714.1:c.1964G>T	ENSP00000514539.1:p.Cys655Phe
ENST00000699715.1:c.1964G>T	ENSP00000514540.1:p.Cys655Phe
ENST00000699716.1:c.1964G>T	ENSP00000514542.1:p.Cys655Phe
ENST00000699717.1:n.1690G>T
ENST00000699718.1:c.3362G>T	ENSP00000514543.1:p.Cys1121Phe
ENST00000462833.6:c.3287G>T MANE Select	ENSP00000419361.1:p.Cys1096Phe
ENST00000309879.9:c.2237G>T	ENSP00000308685.5:p.Cys746Phe
ENST00000462833.5:c.3287G>T	ENSP00000419361.1:p.Cys1096Phe
ENST00000491190.5:c.2261G>T	ENSP00000418537.1:p.Cys754Phe
NM_001199642.1:c.2237G>T	NP_001186571.1:p.Cys746Phe
NM_183357.2:c.3287G>T	NP_899200.1:p.Cys1096Phe
XM_005247077.2:c.3362G>T	XP_005247134.1:p.Cys1121Phe
XM_005247078.1:c.2312G>T	XP_005247135.1:p.Cys771Phe
XM_006713483.1:c.2261G>T	XP_006713546.1:p.Cys754Phe
XM_006713484.1:c.2039G>T	XP_006713547.1:p.Cys680Phe
XM_011512359.1:c.2363G>T	XP_011510661.1:p.Cys788Phe
XM_011512360.1:c.2273G>T	XP_011510662.1:p.Cys758Phe
XM_011512361.1:c.2039G>T	XP_011510663.1:p.Cys680Phe
XM_005247077.4:c.3362G>T	XP_005247134.1:p.Cys1121Phe
XM_011512359.2:c.2363G>T	XP_011510661.1:p.Cys788Phe
XM_011512360.3:c.2273G>T	XP_011510662.1:p.Cys758Phe
XM_017005638.1:c.2264G>T	XP_016861127.1:p.Cys755Phe
XM_017005639.1:c.2264G>T	XP_016861128.1:p.Cys755Phe
NM_001378259.1:c.3362G>T	NP_001365188.1:p.Cys1121Phe
NM_183357.3:c.3287G>T MANE Select	NP_899200.1:p.Cys1096Phe