Canonical Allele Identifier: CA354218234

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123044170A>C (hg19) ; chr3:g.123325323A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123325323A>C , CM000665.2:g.123325323A>C	GRCh38
NC_000003.11:g.123044170A>C , CM000665.1:g.123044170A>C	GRCh37
NC_000003.10:g.124526860A>C	NCBI36
NG_033882.1:g.128223T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.764T>G	ENSP00000420082.2:p.Met255Arg
ENST00000470367.2:c.1052T>G	ENSP00000514541.1:p.Met351Arg
ENST00000483566.2:c.764T>G	ENSP00000420252.2:p.Met255Arg
ENST00000699714.1:c.764T>G	ENSP00000514539.1:p.Met255Arg
ENST00000699715.1:c.764T>G	ENSP00000514540.1:p.Met255Arg
ENST00000699716.1:c.764T>G	ENSP00000514542.1:p.Met255Arg
ENST00000699718.1:c.2087T>G	ENSP00000514543.1:p.Met696Arg
ENST00000699719.1:n.346T>G
ENST00000462833.6:c.2087T>G MANE Select	ENSP00000419361.1:p.Met696Arg
ENST00000309879.9:c.1037T>G	ENSP00000308685.5:p.Met346Arg
ENST00000462833.5:c.2087T>G	ENSP00000419361.1:p.Met696Arg
ENST00000466617.5:c.764T>G	ENSP00000420082.1:p.Met255Arg
ENST00000491190.5:c.986T>G	ENSP00000418537.1:p.Met329Arg
NM_001199642.1:c.1037T>G	NP_001186571.1:p.Met346Arg
NM_183357.2:c.2087T>G	NP_899200.1:p.Met696Arg
XM_005247077.2:c.2087T>G	XP_005247134.1:p.Met696Arg
XM_005247078.1:c.1037T>G	XP_005247135.1:p.Met346Arg
XM_006713483.1:c.986T>G	XP_006713546.1:p.Met329Arg
XM_006713484.1:c.764T>G	XP_006713547.1:p.Met255Arg
XM_011512358.1:c.2087T>G	XP_011510660.1:p.Met696Arg
XM_011512359.1:c.1088T>G	XP_011510661.1:p.Met363Arg
XM_011512360.1:c.998T>G	XP_011510662.1:p.Met333Arg
XM_011512361.1:c.764T>G	XP_011510663.1:p.Met255Arg
XM_005247077.4:c.2087T>G	XP_005247134.1:p.Met696Arg
XM_011512359.2:c.1088T>G	XP_011510661.1:p.Met363Arg
XM_011512360.3:c.998T>G	XP_011510662.1:p.Met333Arg
XM_017005638.1:c.989T>G	XP_016861127.1:p.Met330Arg
XM_017005639.1:c.989T>G	XP_016861128.1:p.Met330Arg
NM_001378259.1:c.2087T>G	NP_001365188.1:p.Met696Arg
NM_183357.3:c.2087T>G MANE Select	NP_899200.1:p.Met696Arg