Canonical Allele Identifier: CA2667291966

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123284642-GTCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284648_123284650del , CM000665.2:g.123284648_123284650del	GRCh38
NC_000003.11:g.123003495_123003497del , CM000665.1:g.123003495_123003497del	GRCh37
NC_000003.10:g.124486185_124486187del	NCBI36
NG_033882.1:g.168901_168903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2426_2428del	ENSP00000420082.2:p.Met809del
ENST00000470367.2:c.2714_2716del	ENSP00000514541.1:p.Met905del
ENST00000483566.2:c.2426_2428del	ENSP00000420252.2:p.Met809del
ENST00000699714.1:c.2426_2428del	ENSP00000514539.1:p.Met809del
ENST00000699715.1:c.2426_2428del	ENSP00000514540.1:p.Met809del
ENST00000699716.1:c.2426_2428del	ENSP00000514542.1:p.Met809del
ENST00000699717.1:n.2152_2154del
ENST00000699718.1:c.3824_3826del	ENSP00000514543.1:p.Met1275del
ENST00000462833.6:c.3749_3751del MANE Select	ENSP00000419361.1:p.Met1250del
ENST00000309879.9:c.2699_2701del	ENSP00000308685.5:p.Met900del
ENST00000462833.5:c.3749_3751del	ENSP00000419361.1:p.Met1250del
ENST00000478092.1:n.519_521del
ENST00000491190.5:c.2723_2725del	ENSP00000418537.1:p.Met908del
NM_001199642.1:c.2699_2701del	NP_001186571.1:p.Met900del
NM_183357.2:c.3749_3751del	NP_899200.1:p.Met1250del
XM_005247077.2:c.3824_3826del	XP_005247134.1:p.Met1275del
XM_005247078.1:c.2774_2776del	XP_005247135.1:p.Met925del
XM_006713483.1:c.2723_2725del	XP_006713546.1:p.Met908del
XM_006713484.1:c.2501_2503del	XP_006713547.1:p.Met834del
XM_011512359.1:c.2825_2827del	XP_011510661.1:p.Met942del
XM_011512360.1:c.2735_2737del	XP_011510662.1:p.Met912del
XM_011512361.1:c.2501_2503del	XP_011510663.1:p.Met834del
XM_005247077.4:c.3824_3826del	XP_005247134.1:p.Met1275del
XM_011512359.2:c.2825_2827del	XP_011510661.1:p.Met942del
XM_011512360.3:c.2735_2737del	XP_011510662.1:p.Met912del
XM_017005638.1:c.2726_2728del	XP_016861127.1:p.Met909del
XM_017005639.1:c.2726_2728del	XP_016861128.1:p.Met909del
NM_001378259.1:c.3824_3826del	NP_001365188.1:p.Met1275del
NM_183357.3:c.3749_3751del MANE Select	NP_899200.1:p.Met1250del