Canonical Allele Identifier: CA2543213341

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123325483_123325484insCAGCCT , CM000665.2:g.123325483_123325484insCAGCCT	GRCh38
NC_000003.11:g.123044330_123044331insCAGCCT , CM000665.1:g.123044330_123044331insCAGCCT	GRCh37
NC_000003.10:g.124527020_124527021insCAGCCT	NCBI36
NG_033882.1:g.128063_128064insGGCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.625-21_625-20insGGCTGA	ENSP00000420082.2:n.625-21_625-20insGGCTGA
ENST00000470367.2:c.913-21_913-20insGGCTGA	ENSP00000514541.1:n.913-21_913-20insGGCTGA
ENST00000483566.2:c.625-21_625-20insGGCTGA	ENSP00000420252.2:n.625-21_625-20insGGCTGA
ENST00000699714.1:c.625-21_625-20insGGCTGA	ENSP00000514539.1:n.625-21_625-20insGGCTGA
ENST00000699715.1:c.625-21_625-20insGGCTGA	ENSP00000514540.1:n.625-21_625-20insGGCTGA
ENST00000699716.1:c.625-21_625-20insGGCTGA	ENSP00000514542.1:n.625-21_625-20insGGCTGA
ENST00000699718.1:c.1948-21_1948-20insGGCTGA	ENSP00000514543.1:n.1948-21_1948-20insGGCTGA
ENST00000699719.1:n.207-21_207-20insGGCTGA
ENST00000462833.6:c.1948-21_1948-20insGGCTGA MANE Select	ENSP00000419361.1:n.1948-21_1948-20insGGCTGA
ENST00000309879.9:c.898-21_898-20insGGCTGA	ENSP00000308685.5:n.898-21_898-20insGGCTGA
ENST00000462833.5:c.1948-21_1948-20insGGCTGA	ENSP00000419361.1:n.1948-21_1948-20insGGCTGA
ENST00000466617.5:c.625-21_625-20insGGCTGA	ENSP00000420082.1:n.625-21_625-20insGGCTGA
ENST00000491190.5:c.847-21_847-20insGGCTGA	ENSP00000418537.1:n.847-21_847-20insGGCTGA
NM_001199642.1:c.898-21_898-20insGGCTGA	NP_001186571.1:n.898-21_898-20insGGCTGA
NM_183357.2:c.1948-21_1948-20insGGCTGA	NP_899200.1:n.1948-21_1948-20insGGCTGA
XM_005247077.2:c.1948-21_1948-20insGGCTGA	XP_005247134.1:n.1948-21_1948-20insGGCTGA
XM_005247078.1:c.898-21_898-20insGGCTGA	XP_005247135.1:n.898-21_898-20insGGCTGA
XM_006713483.1:c.847-21_847-20insGGCTGA	XP_006713546.1:n.847-21_847-20insGGCTGA
XM_006713484.1:c.625-21_625-20insGGCTGA	XP_006713547.1:n.625-21_625-20insGGCTGA
XM_011512358.1:c.1948-21_1948-20insGGCTGA	XP_011510660.1:n.1948-21_1948-20insGGCTGA
XM_011512359.1:c.949-21_949-20insGGCTGA	XP_011510661.1:n.949-21_949-20insGGCTGA
XM_011512360.1:c.859-21_859-20insGGCTGA	XP_011510662.1:n.859-21_859-20insGGCTGA
XM_011512361.1:c.625-21_625-20insGGCTGA	XP_011510663.1:n.625-21_625-20insGGCTGA
XM_005247077.4:c.1948-21_1948-20insGGCTGA	XP_005247134.1:n.1948-21_1948-20insGGCTGA
XM_011512359.2:c.949-21_949-20insGGCTGA	XP_011510661.1:n.949-21_949-20insGGCTGA
XM_011512360.3:c.859-21_859-20insGGCTGA	XP_011510662.1:n.859-21_859-20insGGCTGA
XM_017005638.1:c.850-21_850-20insGGCTGA	XP_016861127.1:n.850-21_850-20insGGCTGA
XM_017005639.1:c.850-21_850-20insGGCTGA	XP_016861128.1:n.850-21_850-20insGGCTGA
NM_001378259.1:c.1948-21_1948-20insGGCTGA	NP_001365188.1:n.1948-21_1948-20insGGCTGA
NM_183357.3:c.1948-21_1948-20insGGCTGA MANE Select	NP_899200.1:n.1948-21_1948-20insGGCTGA