Canonical Allele Identifier: CA1053003751

Gene: ADCY5

Linked Data

• gnomAD v3: 3-123319376-GAA-G
• gnomAD v4: 3-123319376-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123319386_123319387del , CM000665.2:g.123319386_123319387del	GRCh38
NC_000003.11:g.123038233_123038234del , CM000665.1:g.123038233_123038234del	GRCh37
NC_000003.10:g.124520923_124520924del	NCBI36
NG_033882.1:g.134168_134169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.933+296_933+297del	ENSP00000420082.2:n.933+296_933+297del
ENST00000470367.2:c.1221+296_1221+297del	ENSP00000514541.1:n.1221+296_1221+297del
ENST00000483566.2:c.933+296_933+297del	ENSP00000420252.2:n.933+296_933+297del
ENST00000699714.1:c.933+296_933+297del	ENSP00000514539.1:n.933+296_933+297del
ENST00000699715.1:c.933+296_933+297del	ENSP00000514540.1:n.933+296_933+297del
ENST00000699716.1:c.933+296_933+297del	ENSP00000514542.1:n.933+296_933+297del
ENST00000699718.1:c.2256+296_2256+297del	ENSP00000514543.1:n.2256+296_2256+297del
ENST00000699719.1:n.515+296_515+297del
ENST00000462833.6:c.2256+296_2256+297del MANE Select	ENSP00000419361.1:n.2256+296_2256+297del
ENST00000309879.9:c.1206+296_1206+297del	ENSP00000308685.5:n.1206+296_1206+297del
ENST00000462833.5:c.2256+296_2256+297del	ENSP00000419361.1:n.2256+296_2256+297del
ENST00000466617.5:c.933+296_933+297del	ENSP00000420082.1:n.933+296_933+297del
ENST00000491190.5:c.1155+296_1155+297del	ENSP00000418537.1:n.1155+296_1155+297del
NM_001199642.1:c.1206+296_1206+297del	NP_001186571.1:n.1206+296_1206+297del
NM_183357.2:c.2256+296_2256+297del	NP_899200.1:n.2256+296_2256+297del
XM_005247077.2:c.2256+296_2256+297del	XP_005247134.1:n.2256+296_2256+297del
XM_005247078.1:c.1206+296_1206+297del	XP_005247135.1:n.1206+296_1206+297del
XM_006713483.1:c.1155+296_1155+297del	XP_006713546.1:n.1155+296_1155+297del
XM_006713484.1:c.933+296_933+297del	XP_006713547.1:n.933+296_933+297del
XM_011512358.1:c.2256+296_2256+297del	XP_011510660.1:n.2256+296_2256+297del
XM_011512359.1:c.1257+296_1257+297del	XP_011510661.1:n.1257+296_1257+297del
XM_011512360.1:c.1167+296_1167+297del	XP_011510662.1:n.1167+296_1167+297del
XM_011512361.1:c.933+296_933+297del	XP_011510663.1:n.933+296_933+297del
XM_005247077.4:c.2256+296_2256+297del	XP_005247134.1:n.2256+296_2256+297del
XM_011512359.2:c.1257+296_1257+297del	XP_011510661.1:n.1257+296_1257+297del
XM_011512360.3:c.1167+296_1167+297del	XP_011510662.1:n.1167+296_1167+297del
XM_017005638.1:c.1158+296_1158+297del	XP_016861127.1:n.1158+296_1158+297del
XM_017005639.1:c.1158+296_1158+297del	XP_016861128.1:n.1158+296_1158+297del
NM_001378259.1:c.2256+296_2256+297del	NP_001365188.1:n.2256+296_2256+297del
NM_183357.3:c.2256+296_2256+297del MANE Select	NP_899200.1:n.2256+296_2256+297del