Canonical Allele Identifier: CA1398327488

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284723A= , CM000665.2:g.123284723A=	GRCh38
NC_000003.11:g.123003570A= , CM000665.1:g.123003570A=	GRCh37
NC_000003.10:g.124486260A=	NCBI36
NG_033882.1:g.168823T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2348T=	ENSP00000420082.2:p.Met783=
ENST00000470367.2:c.2636T=	ENSP00000514541.1:p.Met879=
ENST00000483566.2:c.2348T=	ENSP00000420252.2:p.Met783=
ENST00000699714.1:c.2348T=	ENSP00000514539.1:p.Met783=
ENST00000699715.1:c.2348T=	ENSP00000514540.1:p.Met783=
ENST00000699716.1:c.2348T=	ENSP00000514542.1:p.Met783=
ENST00000699717.1:n.2074T=
ENST00000699718.1:c.3746T=	ENSP00000514543.1:p.Met1249=
ENST00000462833.6:c.3671T= MANE Select	ENSP00000419361.1:p.Met1224=
ENST00000309879.9:c.2621T=	ENSP00000308685.5:p.Met874=
ENST00000462833.5:c.3671T=	ENSP00000419361.1:p.Met1224=
ENST00000478092.1:n.441T=
ENST00000491190.5:c.2645T=	ENSP00000418537.1:p.Met882=
NM_001199642.1:c.2621T=	NP_001186571.1:p.Met874=
NM_183357.2:c.3671T=	NP_899200.1:p.Met1224=
XM_005247077.2:c.3746T=	XP_005247134.1:p.Met1249=
XM_005247078.1:c.2696T=	XP_005247135.1:p.Met899=
XM_006713483.1:c.2645T=	XP_006713546.1:p.Met882=
XM_006713484.1:c.2423T=	XP_006713547.1:p.Met808=
XM_011512359.1:c.2747T=	XP_011510661.1:p.Met916=
XM_011512360.1:c.2657T=	XP_011510662.1:p.Met886=
XM_011512361.1:c.2423T=	XP_011510663.1:p.Met808=
XM_005247077.4:c.3746T=	XP_005247134.1:p.Met1249=
XM_011512359.2:c.2747T=	XP_011510661.1:p.Met916=
XM_011512360.3:c.2657T=	XP_011510662.1:p.Met886=
XM_017005638.1:c.2648T=	XP_016861127.1:p.Met883=
XM_017005639.1:c.2648T=	XP_016861128.1:p.Met883=
NM_001378259.1:c.3746T=	NP_001365188.1:p.Met1249=
NM_183357.3:c.3671T= MANE Select	NP_899200.1:p.Met1224=