Canonical Allele Identifier: CA435297687

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123284677-G-T
• MyVariant Identifiers: chr3:g.123003524G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284677G>T , CM000665.2:g.123284677G>T	GRCh38
NC_000003.11:g.123003524G>T , CM000665.1:g.123003524G>T	GRCh37
NC_000003.10:g.124486214G>T	NCBI36
NG_033882.1:g.168869C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2394C>A	ENSP00000420082.2:p.Gly798=
ENST00000470367.2:c.2682C>A	ENSP00000514541.1:p.Gly894=
ENST00000483566.2:c.2394C>A	ENSP00000420252.2:p.Gly798=
ENST00000699714.1:c.2394C>A	ENSP00000514539.1:p.Gly798=
ENST00000699715.1:c.2394C>A	ENSP00000514540.1:p.Gly798=
ENST00000699716.1:c.2394C>A	ENSP00000514542.1:p.Gly798=
ENST00000699717.1:n.2120C>A
ENST00000699718.1:c.3792C>A	ENSP00000514543.1:p.Gly1264=
ENST00000462833.6:c.3717C>A MANE Select	ENSP00000419361.1:p.Gly1239=
ENST00000309879.9:c.2667C>A	ENSP00000308685.5:p.Gly889=
ENST00000462833.5:c.3717C>A	ENSP00000419361.1:p.Gly1239=
ENST00000478092.1:n.487C>A
ENST00000491190.5:c.2691C>A	ENSP00000418537.1:p.Gly897=
NM_001199642.1:c.2667C>A	NP_001186571.1:p.Gly889=
NM_183357.2:c.3717C>A	NP_899200.1:p.Gly1239=
XM_005247077.2:c.3792C>A	XP_005247134.1:p.Gly1264=
XM_005247078.1:c.2742C>A	XP_005247135.1:p.Gly914=
XM_006713483.1:c.2691C>A	XP_006713546.1:p.Gly897=
XM_006713484.1:c.2469C>A	XP_006713547.1:p.Gly823=
XM_011512359.1:c.2793C>A	XP_011510661.1:p.Gly931=
XM_011512360.1:c.2703C>A	XP_011510662.1:p.Gly901=
XM_011512361.1:c.2469C>A	XP_011510663.1:p.Gly823=
XM_005247077.4:c.3792C>A	XP_005247134.1:p.Gly1264=
XM_011512359.2:c.2793C>A	XP_011510661.1:p.Gly931=
XM_011512360.3:c.2703C>A	XP_011510662.1:p.Gly901=
XM_017005638.1:c.2694C>A	XP_016861127.1:p.Gly898=
XM_017005639.1:c.2694C>A	XP_016861128.1:p.Gly898=
NM_001378259.1:c.3792C>A	NP_001365188.1:p.Gly1264=
NM_183357.3:c.3717C>A MANE Select	NP_899200.1:p.Gly1239=