Canonical Allele Identifier: CA354222144

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003565G>T (hg19) ; chr3:g.123284718G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284718G>T , CM000665.2:g.123284718G>T	GRCh38
NC_000003.11:g.123003565G>T , CM000665.1:g.123003565G>T	GRCh37
NC_000003.10:g.124486255G>T	NCBI36
NG_033882.1:g.168828C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2353C>A	ENSP00000420082.2:p.Gln785Lys
ENST00000470367.2:c.2641C>A	ENSP00000514541.1:p.Gln881Lys
ENST00000483566.2:c.2353C>A	ENSP00000420252.2:p.Gln785Lys
ENST00000699714.1:c.2353C>A	ENSP00000514539.1:p.Gln785Lys
ENST00000699715.1:c.2353C>A	ENSP00000514540.1:p.Gln785Lys
ENST00000699716.1:c.2353C>A	ENSP00000514542.1:p.Gln785Lys
ENST00000699717.1:n.2079C>A
ENST00000699718.1:c.3751C>A	ENSP00000514543.1:p.Gln1251Lys
ENST00000462833.6:c.3676C>A MANE Select	ENSP00000419361.1:p.Gln1226Lys
ENST00000309879.9:c.2626C>A	ENSP00000308685.5:p.Gln876Lys
ENST00000462833.5:c.3676C>A	ENSP00000419361.1:p.Gln1226Lys
ENST00000478092.1:n.446C>A
ENST00000491190.5:c.2650C>A	ENSP00000418537.1:p.Gln884Lys
NM_001199642.1:c.2626C>A	NP_001186571.1:p.Gln876Lys
NM_183357.2:c.3676C>A	NP_899200.1:p.Gln1226Lys
XM_005247077.2:c.3751C>A	XP_005247134.1:p.Gln1251Lys
XM_005247078.1:c.2701C>A	XP_005247135.1:p.Gln901Lys
XM_006713483.1:c.2650C>A	XP_006713546.1:p.Gln884Lys
XM_006713484.1:c.2428C>A	XP_006713547.1:p.Gln810Lys
XM_011512359.1:c.2752C>A	XP_011510661.1:p.Gln918Lys
XM_011512360.1:c.2662C>A	XP_011510662.1:p.Gln888Lys
XM_011512361.1:c.2428C>A	XP_011510663.1:p.Gln810Lys
XM_005247077.4:c.3751C>A	XP_005247134.1:p.Gln1251Lys
XM_011512359.2:c.2752C>A	XP_011510661.1:p.Gln918Lys
XM_011512360.3:c.2662C>A	XP_011510662.1:p.Gln888Lys
XM_017005638.1:c.2653C>A	XP_016861127.1:p.Gln885Lys
XM_017005639.1:c.2653C>A	XP_016861128.1:p.Gln885Lys
NM_001378259.1:c.3751C>A	NP_001365188.1:p.Gln1251Lys
NM_183357.3:c.3676C>A MANE Select	NP_899200.1:p.Gln1226Lys