Canonical Allele Identifier: CA1398330348

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291097_123291098delinsAG , CM000665.2:g.123291097_123291098delinsAG	GRCh38
NC_000003.11:g.123009944_123009945delinsAG , CM000665.1:g.123009944_123009945delinsAG	GRCh37
NC_000003.10:g.124492634_124492635delinsAG	NCBI36
NG_033882.1:g.162448_162449delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2004+15_2004+16delinsCT	ENSP00000420082.2:n.2004+15_2004+16delinsCT
ENST00000470367.2:c.2292+15_2292+16delinsCT	ENSP00000514541.1:n.2292+15_2292+16delinsCT
ENST00000483566.2:c.2004+15_2004+16delinsCT	ENSP00000420252.2:n.2004+15_2004+16delinsCT
ENST00000699714.1:c.2004+15_2004+16delinsCT	ENSP00000514539.1:n.2004+15_2004+16delinsCT
ENST00000699715.1:c.2004+15_2004+16delinsCT	ENSP00000514540.1:n.2004+15_2004+16delinsCT
ENST00000699716.1:c.2004+15_2004+16delinsCT	ENSP00000514542.1:n.2004+15_2004+16delinsCT
ENST00000699717.1:n.1730+15_1730+16delinsCT
ENST00000699718.1:c.3402+15_3402+16delinsCT	ENSP00000514543.1:n.3402+15_3402+16delinsCT
ENST00000462833.6:c.3327+15_3327+16delinsCT MANE Select	ENSP00000419361.1:n.3327+15_3327+16delinsCT
ENST00000309879.9:c.2277+15_2277+16delinsCT	ENSP00000308685.5:n.2277+15_2277+16delinsCT
ENST00000462833.5:c.3327+15_3327+16delinsCT	ENSP00000419361.1:n.3327+15_3327+16delinsCT
ENST00000491190.5:c.2301+15_2301+16delinsCT	ENSP00000418537.1:n.2301+15_2301+16delinsCT
NM_001199642.1:c.2277+15_2277+16delinsCT	NP_001186571.1:n.2277+15_2277+16delinsCT
NM_183357.2:c.3327+15_3327+16delinsCT	NP_899200.1:n.3327+15_3327+16delinsCT
XM_005247077.2:c.3402+15_3402+16delinsCT	XP_005247134.1:n.3402+15_3402+16delinsCT
XM_005247078.1:c.2352+15_2352+16delinsCT	XP_005247135.1:n.2352+15_2352+16delinsCT
XM_006713483.1:c.2301+15_2301+16delinsCT	XP_006713546.1:n.2301+15_2301+16delinsCT
XM_006713484.1:c.2079+15_2079+16delinsCT	XP_006713547.1:n.2079+15_2079+16delinsCT
XM_011512359.1:c.2403+15_2403+16delinsCT	XP_011510661.1:n.2403+15_2403+16delinsCT
XM_011512360.1:c.2313+15_2313+16delinsCT	XP_011510662.1:n.2313+15_2313+16delinsCT
XM_011512361.1:c.2079+15_2079+16delinsCT	XP_011510663.1:n.2079+15_2079+16delinsCT
XM_005247077.4:c.3402+15_3402+16delinsCT	XP_005247134.1:n.3402+15_3402+16delinsCT
XM_011512359.2:c.2403+15_2403+16delinsCT	XP_011510661.1:n.2403+15_2403+16delinsCT
XM_011512360.3:c.2313+15_2313+16delinsCT	XP_011510662.1:n.2313+15_2313+16delinsCT
XM_017005638.1:c.2304+15_2304+16delinsCT	XP_016861127.1:n.2304+15_2304+16delinsCT
XM_017005639.1:c.2304+15_2304+16delinsCT	XP_016861128.1:n.2304+15_2304+16delinsCT
NM_001378259.1:c.3402+15_3402+16delinsCT	NP_001365188.1:n.3402+15_3402+16delinsCT
NM_183357.3:c.3327+15_3327+16delinsCT MANE Select	NP_899200.1:n.3327+15_3327+16delinsCT