Canonical Allele Identifier: CA435296424

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123071288G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123352441G>A , CM000665.2:g.123352441G>A	GRCh38
NC_000003.11:g.123071288G>A , CM000665.1:g.123071288G>A	GRCh37
NC_000003.10:g.124553978G>A	NCBI36
NG_033882.1:g.101105C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.-49C>T	ENSP00000420082.2:n.-49C>T
ENST00000470367.2:c.240C>T	ENSP00000514541.1:p.Asn80=
ENST00000483566.2:c.-49C>T	ENSP00000420252.2:n.-49C>T
ENST00000699714.1:c.-49C>T	ENSP00000514539.1:n.-49C>T
ENST00000699715.1:c.-49C>T	ENSP00000514540.1:n.-49C>T
ENST00000699716.1:c.-49C>T	ENSP00000514542.1:n.-49C>T
ENST00000699718.1:c.1275C>T	ENSP00000514543.1:p.Asn425=
ENST00000462833.6:c.1275C>T MANE Select	ENSP00000419361.1:p.Asn425=
ENST00000309879.9:c.225C>T	ENSP00000308685.5:p.Asn75=
ENST00000462833.5:c.1275C>T	ENSP00000419361.1:p.Asn425=
ENST00000466617.5:c.-49C>T	ENSP00000420082.1:n.-49C>T
ENST00000476455.1:c.179C>T	ENSP00000417789.1:p.Thr60Ile
ENST00000483566.1:c.-49C>T	ENSP00000420252.1:n.-49C>T
ENST00000491190.5:c.174C>T	ENSP00000418537.1:p.Asn58=
NM_001199642.1:c.225C>T	NP_001186571.1:p.Asn75=
NM_183357.2:c.1275C>T	NP_899200.1:p.Asn425=
XM_005247077.2:c.1275C>T	XP_005247134.1:p.Asn425=
XM_005247078.1:c.225C>T	XP_005247135.1:p.Asn75=
XM_006713483.1:c.174C>T	XP_006713546.1:p.Asn58=
XM_006713484.1:c.-49C>T	XP_006713547.1:n.-49C>T
XM_011512358.1:c.1275C>T	XP_011510660.1:p.Asn425=
XM_011512359.1:c.276C>T	XP_011510661.1:p.Asn92=
XM_011512360.1:c.186C>T	XP_011510662.1:p.Asn62=
XM_011512361.1:c.-49C>T	XP_011510663.1:n.-49C>T
XM_005247077.4:c.1275C>T	XP_005247134.1:p.Asn425=
XM_011512359.2:c.276C>T	XP_011510661.1:p.Asn92=
XM_011512360.3:c.186C>T	XP_011510662.1:p.Asn62=
XM_017005638.1:c.177C>T	XP_016861127.1:p.Asn59=
XM_017005639.1:c.177C>T	XP_016861128.1:p.Asn59=
NM_001378259.1:c.1275C>T	NP_001365188.1:p.Asn425=
NM_183357.3:c.1275C>T MANE Select	NP_899200.1:p.Asn425=