Canonical Allele Identifier: CA435297698

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003542G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284695G>A , CM000665.2:g.123284695G>A	GRCh38
NC_000003.11:g.123003542G>A , CM000665.1:g.123003542G>A	GRCh37
NC_000003.10:g.124486232G>A	NCBI36
NG_033882.1:g.168851C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2376C>T	ENSP00000420082.2:p.Tyr792=
ENST00000470367.2:c.2664C>T	ENSP00000514541.1:p.Tyr888=
ENST00000483566.2:c.2376C>T	ENSP00000420252.2:p.Tyr792=
ENST00000699714.1:c.2376C>T	ENSP00000514539.1:p.Tyr792=
ENST00000699715.1:c.2376C>T	ENSP00000514540.1:p.Tyr792=
ENST00000699716.1:c.2376C>T	ENSP00000514542.1:p.Tyr792=
ENST00000699717.1:n.2102C>T
ENST00000699718.1:c.3774C>T	ENSP00000514543.1:p.Tyr1258=
ENST00000462833.6:c.3699C>T MANE Select	ENSP00000419361.1:p.Tyr1233=
ENST00000309879.9:c.2649C>T	ENSP00000308685.5:p.Tyr883=
ENST00000462833.5:c.3699C>T	ENSP00000419361.1:p.Tyr1233=
ENST00000478092.1:n.469C>T
ENST00000491190.5:c.2673C>T	ENSP00000418537.1:p.Tyr891=
NM_001199642.1:c.2649C>T	NP_001186571.1:p.Tyr883=
NM_183357.2:c.3699C>T	NP_899200.1:p.Tyr1233=
XM_005247077.2:c.3774C>T	XP_005247134.1:p.Tyr1258=
XM_005247078.1:c.2724C>T	XP_005247135.1:p.Tyr908=
XM_006713483.1:c.2673C>T	XP_006713546.1:p.Tyr891=
XM_006713484.1:c.2451C>T	XP_006713547.1:p.Tyr817=
XM_011512359.1:c.2775C>T	XP_011510661.1:p.Tyr925=
XM_011512360.1:c.2685C>T	XP_011510662.1:p.Tyr895=
XM_011512361.1:c.2451C>T	XP_011510663.1:p.Tyr817=
XM_005247077.4:c.3774C>T	XP_005247134.1:p.Tyr1258=
XM_011512359.2:c.2775C>T	XP_011510661.1:p.Tyr925=
XM_011512360.3:c.2685C>T	XP_011510662.1:p.Tyr895=
XM_017005638.1:c.2676C>T	XP_016861127.1:p.Tyr892=
XM_017005639.1:c.2676C>T	XP_016861128.1:p.Tyr892=
NM_001378259.1:c.3774C>T	NP_001365188.1:p.Tyr1258=
NM_183357.3:c.3699C>T MANE Select	NP_899200.1:p.Tyr1233=