Canonical Allele Identifier: CA1398330434

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291305G= , CM000665.2:g.123291305G=	GRCh38
NC_000003.11:g.123010152G= , CM000665.1:g.123010152G=	GRCh37
NC_000003.10:g.124492842G=	NCBI36
NG_033882.1:g.162241C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1812C=	ENSP00000420082.2:p.Pro604=
ENST00000470367.2:c.2100C=	ENSP00000514541.1:p.Pro700=
ENST00000483566.2:c.1812C=	ENSP00000420252.2:p.Pro604=
ENST00000699714.1:c.1812C=	ENSP00000514539.1:p.Pro604=
ENST00000699715.1:c.1812C=	ENSP00000514540.1:p.Pro604=
ENST00000699716.1:c.1812C=	ENSP00000514542.1:p.Pro604=
ENST00000699717.1:n.1538C=
ENST00000699718.1:c.3210C=	ENSP00000514543.1:p.Pro1070=
ENST00000462833.6:c.3135C= MANE Select	ENSP00000419361.1:p.Pro1045=
ENST00000309879.9:c.2085C=	ENSP00000308685.5:p.Pro695=
ENST00000462833.5:c.3135C=	ENSP00000419361.1:p.Pro1045=
ENST00000491190.5:c.2109C=	ENSP00000418537.1:p.Pro703=
NM_001199642.1:c.2085C=	NP_001186571.1:p.Pro695=
NM_183357.2:c.3135C=	NP_899200.1:p.Pro1045=
XM_005247077.2:c.3210C=	XP_005247134.1:p.Pro1070=
XM_005247078.1:c.2160C=	XP_005247135.1:p.Pro720=
XM_006713483.1:c.2109C=	XP_006713546.1:p.Pro703=
XM_006713484.1:c.1887C=	XP_006713547.1:p.Pro629=
XM_011512359.1:c.2211C=	XP_011510661.1:p.Pro737=
XM_011512360.1:c.2121C=	XP_011510662.1:p.Pro707=
XM_011512361.1:c.1887C=	XP_011510663.1:p.Pro629=
XM_005247077.4:c.3210C=	XP_005247134.1:p.Pro1070=
XM_011512359.2:c.2211C=	XP_011510661.1:p.Pro737=
XM_011512360.3:c.2121C=	XP_011510662.1:p.Pro707=
XM_017005638.1:c.2112C=	XP_016861127.1:p.Pro704=
XM_017005639.1:c.2112C=	XP_016861128.1:p.Pro704=
NM_001378259.1:c.3210C=	NP_001365188.1:p.Pro1070=
NM_183357.3:c.3135C= MANE Select	NP_899200.1:p.Pro1045=