Canonical Allele Identifier: CA354221769

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003471C>T (hg19) ; chr3:g.123284624C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284624C>T , CM000665.2:g.123284624C>T	GRCh38
NC_000003.11:g.123003471C>T , CM000665.1:g.123003471C>T	GRCh37
NC_000003.10:g.124486161C>T	NCBI36
NG_033882.1:g.168922G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2447G>A	ENSP00000420082.2:p.Gly816Glu
ENST00000470367.2:c.2735G>A	ENSP00000514541.1:p.Gly912Glu
ENST00000483566.2:c.2447G>A	ENSP00000420252.2:p.Gly816Glu
ENST00000699714.1:c.2447G>A	ENSP00000514539.1:p.Gly816Glu
ENST00000699715.1:c.2447G>A	ENSP00000514540.1:p.Gly816Glu
ENST00000699716.1:c.2447G>A	ENSP00000514542.1:p.Gly816Glu
ENST00000699717.1:n.2173G>A
ENST00000699718.1:c.3845G>A	ENSP00000514543.1:p.Gly1282Glu
ENST00000462833.6:c.3770G>A MANE Select	ENSP00000419361.1:p.Gly1257Glu
ENST00000309879.9:c.2720G>A	ENSP00000308685.5:p.Gly907Glu
ENST00000462833.5:c.3770G>A	ENSP00000419361.1:p.Gly1257Glu
ENST00000478092.1:n.540G>A
ENST00000491190.5:c.2744G>A	ENSP00000418537.1:p.Gly915Glu
NM_001199642.1:c.2720G>A	NP_001186571.1:p.Gly907Glu
NM_183357.2:c.3770G>A	NP_899200.1:p.Gly1257Glu
XM_005247077.2:c.3845G>A	XP_005247134.1:p.Gly1282Glu
XM_005247078.1:c.2795G>A	XP_005247135.1:p.Gly932Glu
XM_006713483.1:c.2744G>A	XP_006713546.1:p.Gly915Glu
XM_006713484.1:c.2522G>A	XP_006713547.1:p.Gly841Glu
XM_011512359.1:c.2846G>A	XP_011510661.1:p.Gly949Glu
XM_011512360.1:c.2756G>A	XP_011510662.1:p.Gly919Glu
XM_011512361.1:c.2522G>A	XP_011510663.1:p.Gly841Glu
XM_005247077.4:c.3845G>A	XP_005247134.1:p.Gly1282Glu
XM_011512359.2:c.2846G>A	XP_011510661.1:p.Gly949Glu
XM_011512360.3:c.2756G>A	XP_011510662.1:p.Gly919Glu
XM_017005638.1:c.2747G>A	XP_016861127.1:p.Gly916Glu
XM_017005639.1:c.2747G>A	XP_016861128.1:p.Gly916Glu
NM_001378259.1:c.3845G>A	NP_001365188.1:p.Gly1282Glu
NM_183357.3:c.3770G>A MANE Select	NP_899200.1:p.Gly1257Glu