Canonical Allele Identifier: CA1398330298

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291004_123291006delinsTTA , CM000665.2:g.123291004_123291006delinsTTA	GRCh38
NC_000003.11:g.123009851_123009853delinsTTA , CM000665.1:g.123009851_123009853delinsTTA	GRCh37
NC_000003.10:g.124492541_124492543delinsTTA	NCBI36
NG_033882.1:g.162540_162542delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2004+107_2004+109delinsTAA	ENSP00000420082.2:n.2004+107_2004+109delinsTAA
ENST00000470367.2:c.2292+107_2292+109delinsTAA	ENSP00000514541.1:n.2292+107_2292+109delinsTAA
ENST00000483566.2:c.2004+107_2004+109delinsTAA	ENSP00000420252.2:n.2004+107_2004+109delinsTAA
ENST00000699714.1:c.2004+107_2004+109delinsTAA	ENSP00000514539.1:n.2004+107_2004+109delinsTAA
ENST00000699715.1:c.2004+107_2004+109delinsTAA	ENSP00000514540.1:n.2004+107_2004+109delinsTAA
ENST00000699716.1:c.2004+107_2004+109delinsTAA	ENSP00000514542.1:n.2004+107_2004+109delinsTAA
ENST00000699717.1:n.1730+107_1730+109delinsTAA
ENST00000699718.1:c.3402+107_3402+109delinsTAA	ENSP00000514543.1:n.3402+107_3402+109delinsTAA
ENST00000462833.6:c.3327+107_3327+109delinsTAA MANE Select	ENSP00000419361.1:n.3327+107_3327+109delinsTAA
ENST00000309879.9:c.2277+107_2277+109delinsTAA	ENSP00000308685.5:n.2277+107_2277+109delinsTAA
ENST00000462833.5:c.3327+107_3327+109delinsTAA	ENSP00000419361.1:n.3327+107_3327+109delinsTAA
ENST00000491190.5:c.2301+107_2301+109delinsTAA	ENSP00000418537.1:n.2301+107_2301+109delinsTAA
NM_001199642.1:c.2277+107_2277+109delinsTAA	NP_001186571.1:n.2277+107_2277+109delinsTAA
NM_183357.2:c.3327+107_3327+109delinsTAA	NP_899200.1:n.3327+107_3327+109delinsTAA
XM_005247077.2:c.3402+107_3402+109delinsTAA	XP_005247134.1:n.3402+107_3402+109delinsTAA
XM_005247078.1:c.2352+107_2352+109delinsTAA	XP_005247135.1:n.2352+107_2352+109delinsTAA
XM_006713483.1:c.2301+107_2301+109delinsTAA	XP_006713546.1:n.2301+107_2301+109delinsTAA
XM_006713484.1:c.2079+107_2079+109delinsTAA	XP_006713547.1:n.2079+107_2079+109delinsTAA
XM_011512359.1:c.2403+107_2403+109delinsTAA	XP_011510661.1:n.2403+107_2403+109delinsTAA
XM_011512360.1:c.2313+107_2313+109delinsTAA	XP_011510662.1:n.2313+107_2313+109delinsTAA
XM_011512361.1:c.2079+107_2079+109delinsTAA	XP_011510663.1:n.2079+107_2079+109delinsTAA
XM_005247077.4:c.3402+107_3402+109delinsTAA	XP_005247134.1:n.3402+107_3402+109delinsTAA
XM_011512359.2:c.2403+107_2403+109delinsTAA	XP_011510661.1:n.2403+107_2403+109delinsTAA
XM_011512360.3:c.2313+107_2313+109delinsTAA	XP_011510662.1:n.2313+107_2313+109delinsTAA
XM_017005638.1:c.2304+107_2304+109delinsTAA	XP_016861127.1:n.2304+107_2304+109delinsTAA
XM_017005639.1:c.2304+107_2304+109delinsTAA	XP_016861128.1:n.2304+107_2304+109delinsTAA
NM_001378259.1:c.3402+107_3402+109delinsTAA	NP_001365188.1:n.3402+107_3402+109delinsTAA
NM_183357.3:c.3327+107_3327+109delinsTAA MANE Select	NP_899200.1:n.3327+107_3327+109delinsTAA