Canonical Allele Identifier: CA1398330453

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291354A= , CM000665.2:g.123291354A=	GRCh38
NC_000003.11:g.123010201A= , CM000665.1:g.123010201A=	GRCh37
NC_000003.10:g.124492891A=	NCBI36
NG_033882.1:g.162192T=

Transcript Alleles

HGVS	Amino-acid Change
NM_183357.3:c.3086T= MANE Select	NP_899200.1:p.Met1029=
ENST00000462833.6:c.3086T= MANE Select	ENSP00000419361.1:p.Met1029=
NM_001199642.1:c.2036T=	NP_001186571.1:p.Met679=
NM_001378259.1:c.3161T=	NP_001365188.1:p.Met1054=
NM_183357.2:c.3086T=	NP_899200.1:p.Met1029=
ENST00000309879.9:c.2036T=	ENSP00000308685.5:p.Met679=
ENST00000462833.5:c.3086T=	ENSP00000419361.1:p.Met1029=
ENST00000466617.6:c.1763T=	ENSP00000420082.2:p.Met588=
ENST00000470367.2:c.2051T=	ENSP00000514541.1:p.Met684=
ENST00000483566.2:c.1763T=	ENSP00000420252.2:p.Met588=
ENST00000491190.5:c.2060T=	ENSP00000418537.1:p.Met687=
ENST00000699714.1:c.1763T=	ENSP00000514539.1:p.Met588=
ENST00000699715.1:c.1763T=	ENSP00000514540.1:p.Met588=
ENST00000699716.1:c.1763T=	ENSP00000514542.1:p.Met588=
ENST00000699717.1:n.1489T=
ENST00000699718.1:c.3161T=	ENSP00000514543.1:p.Met1054=
XM_005247077.2:c.3161T=	XP_005247134.1:p.Met1054=
XM_005247077.4:c.3161T=	XP_005247134.1:p.Met1054=
XM_005247078.1:c.2111T=	XP_005247135.1:p.Met704=
XM_006713483.1:c.2060T=	XP_006713546.1:p.Met687=
XM_006713484.1:c.1838T=	XP_006713547.1:p.Met613=
XM_011512359.1:c.2162T=	XP_011510661.1:p.Met721=
XM_011512359.2:c.2162T=	XP_011510661.1:p.Met721=
XM_011512360.1:c.2072T=	XP_011510662.1:p.Met691=
XM_011512360.3:c.2072T=	XP_011510662.1:p.Met691=
XM_011512361.1:c.1838T=	XP_011510663.1:p.Met613=
XM_017005638.1:c.2063T=	XP_016861127.1:p.Met688=
XM_017005639.1:c.2063T=	XP_016861128.1:p.Met688=