Canonical Allele Identifier: CA354217994

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123038640C>T (hg19) ; chr3:g.123319793C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123319793C>T , CM000665.2:g.123319793C>T	GRCh38
NC_000003.11:g.123038640C>T , CM000665.1:g.123038640C>T	GRCh37
NC_000003.10:g.124521330C>T	NCBI36
NG_033882.1:g.133753G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.814G>A	ENSP00000420082.2:p.Glu272Lys
ENST00000470367.2:c.1102G>A	ENSP00000514541.1:p.Glu368Lys
ENST00000483566.2:c.814G>A	ENSP00000420252.2:p.Glu272Lys
ENST00000699714.1:c.814G>A	ENSP00000514539.1:p.Glu272Lys
ENST00000699715.1:c.814G>A	ENSP00000514540.1:p.Glu272Lys
ENST00000699716.1:c.814G>A	ENSP00000514542.1:p.Glu272Lys
ENST00000699718.1:c.2137G>A	ENSP00000514543.1:p.Glu713Lys
ENST00000699719.1:n.396G>A
ENST00000462833.6:c.2137G>A MANE Select	ENSP00000419361.1:p.Glu713Lys
ENST00000309879.9:c.1087G>A	ENSP00000308685.5:p.Glu363Lys
ENST00000462833.5:c.2137G>A	ENSP00000419361.1:p.Glu713Lys
ENST00000466617.5:c.814G>A	ENSP00000420082.1:p.Glu272Lys
ENST00000491190.5:c.1036G>A	ENSP00000418537.1:p.Glu346Lys
NM_001199642.1:c.1087G>A	NP_001186571.1:p.Glu363Lys
NM_183357.2:c.2137G>A	NP_899200.1:p.Glu713Lys
XM_005247077.2:c.2137G>A	XP_005247134.1:p.Glu713Lys
XM_005247078.1:c.1087G>A	XP_005247135.1:p.Glu363Lys
XM_006713483.1:c.1036G>A	XP_006713546.1:p.Glu346Lys
XM_006713484.1:c.814G>A	XP_006713547.1:p.Glu272Lys
XM_011512358.1:c.2137G>A	XP_011510660.1:p.Glu713Lys
XM_011512359.1:c.1138G>A	XP_011510661.1:p.Glu380Lys
XM_011512360.1:c.1048G>A	XP_011510662.1:p.Glu350Lys
XM_011512361.1:c.814G>A	XP_011510663.1:p.Glu272Lys
XM_005247077.4:c.2137G>A	XP_005247134.1:p.Glu713Lys
XM_011512359.2:c.1138G>A	XP_011510661.1:p.Glu380Lys
XM_011512360.3:c.1048G>A	XP_011510662.1:p.Glu350Lys
XM_017005638.1:c.1039G>A	XP_016861127.1:p.Glu347Lys
XM_017005639.1:c.1039G>A	XP_016861128.1:p.Glu347Lys
NM_001378259.1:c.2137G>A	NP_001365188.1:p.Glu713Lys
NM_183357.3:c.2137G>A MANE Select	NP_899200.1:p.Glu713Lys