Canonical Allele Identifier: CA354222169

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003576G>C (hg19) ; chr3:g.123284729G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284729G>C , CM000665.2:g.123284729G>C	GRCh38
NC_000003.11:g.123003576G>C , CM000665.1:g.123003576G>C	GRCh37
NC_000003.10:g.124486266G>C	NCBI36
NG_033882.1:g.168817C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2342C>G	ENSP00000420082.2:p.Thr781Arg
ENST00000470367.2:c.2630C>G	ENSP00000514541.1:p.Thr877Arg
ENST00000483566.2:c.2342C>G	ENSP00000420252.2:p.Thr781Arg
ENST00000699714.1:c.2342C>G	ENSP00000514539.1:p.Thr781Arg
ENST00000699715.1:c.2342C>G	ENSP00000514540.1:p.Thr781Arg
ENST00000699716.1:c.2342C>G	ENSP00000514542.1:p.Thr781Arg
ENST00000699717.1:n.2068C>G
ENST00000699718.1:c.3740C>G	ENSP00000514543.1:p.Thr1247Arg
ENST00000462833.6:c.3665C>G MANE Select	ENSP00000419361.1:p.Thr1222Arg
ENST00000309879.9:c.2615C>G	ENSP00000308685.5:p.Thr872Arg
ENST00000462833.5:c.3665C>G	ENSP00000419361.1:p.Thr1222Arg
ENST00000478092.1:n.435C>G
ENST00000491190.5:c.2639C>G	ENSP00000418537.1:p.Thr880Arg
NM_001199642.1:c.2615C>G	NP_001186571.1:p.Thr872Arg
NM_183357.2:c.3665C>G	NP_899200.1:p.Thr1222Arg
XM_005247077.2:c.3740C>G	XP_005247134.1:p.Thr1247Arg
XM_005247078.1:c.2690C>G	XP_005247135.1:p.Thr897Arg
XM_006713483.1:c.2639C>G	XP_006713546.1:p.Thr880Arg
XM_006713484.1:c.2417C>G	XP_006713547.1:p.Thr806Arg
XM_011512359.1:c.2741C>G	XP_011510661.1:p.Thr914Arg
XM_011512360.1:c.2651C>G	XP_011510662.1:p.Thr884Arg
XM_011512361.1:c.2417C>G	XP_011510663.1:p.Thr806Arg
XM_005247077.4:c.3740C>G	XP_005247134.1:p.Thr1247Arg
XM_011512359.2:c.2741C>G	XP_011510661.1:p.Thr914Arg
XM_011512360.3:c.2651C>G	XP_011510662.1:p.Thr884Arg
XM_017005638.1:c.2642C>G	XP_016861127.1:p.Thr881Arg
XM_017005639.1:c.2642C>G	XP_016861128.1:p.Thr881Arg
NM_001378259.1:c.3740C>G	NP_001365188.1:p.Thr1247Arg
NM_183357.3:c.3665C>G MANE Select	NP_899200.1:p.Thr1222Arg