Canonical Allele Identifier: CA1398343558

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123319722G= , CM000665.2:g.123319722G=	GRCh38
NC_000003.11:g.123038569G= , CM000665.1:g.123038569G=	GRCh37
NC_000003.10:g.124521259G=	NCBI36
NG_033882.1:g.133824C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.885C=	ENSP00000420082.2:p.His295=
ENST00000470367.2:c.1173C=	ENSP00000514541.1:p.His391=
ENST00000483566.2:c.885C=	ENSP00000420252.2:p.His295=
ENST00000699714.1:c.885C=	ENSP00000514539.1:p.His295=
ENST00000699715.1:c.885C=	ENSP00000514540.1:p.His295=
ENST00000699716.1:c.885C=	ENSP00000514542.1:p.His295=
ENST00000699718.1:c.2208C=	ENSP00000514543.1:p.His736=
ENST00000699719.1:n.467C=
ENST00000462833.6:c.2208C= MANE Select	ENSP00000419361.1:p.His736=
ENST00000309879.9:c.1158C=	ENSP00000308685.5:p.His386=
ENST00000462833.5:c.2208C=	ENSP00000419361.1:p.His736=
ENST00000466617.5:c.885C=	ENSP00000420082.1:p.His295=
ENST00000491190.5:c.1107C=	ENSP00000418537.1:p.His369=
NM_001199642.1:c.1158C=	NP_001186571.1:p.His386=
NM_183357.2:c.2208C=	NP_899200.1:p.His736=
XM_005247077.2:c.2208C=	XP_005247134.1:p.His736=
XM_005247078.1:c.1158C=	XP_005247135.1:p.His386=
XM_006713483.1:c.1107C=	XP_006713546.1:p.His369=
XM_006713484.1:c.885C=	XP_006713547.1:p.His295=
XM_011512358.1:c.2208C=	XP_011510660.1:p.His736=
XM_011512359.1:c.1209C=	XP_011510661.1:p.His403=
XM_011512360.1:c.1119C=	XP_011510662.1:p.His373=
XM_011512361.1:c.885C=	XP_011510663.1:p.His295=
XM_005247077.4:c.2208C=	XP_005247134.1:p.His736=
XM_011512359.2:c.1209C=	XP_011510661.1:p.His403=
XM_011512360.3:c.1119C=	XP_011510662.1:p.His373=
XM_017005638.1:c.1110C=	XP_016861127.1:p.His370=
XM_017005639.1:c.1110C=	XP_016861128.1:p.His370=
NM_001378259.1:c.2208C=	NP_001365188.1:p.His736=
NM_183357.3:c.2208C= MANE Select	NP_899200.1:p.His736=