Canonical Allele Identifier: CA354221970

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003513A>C (hg19) ; chr3:g.123284666A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284666A>C , CM000665.2:g.123284666A>C	GRCh38
NC_000003.11:g.123003513A>C , CM000665.1:g.123003513A>C	GRCh37
NC_000003.10:g.124486203A>C	NCBI36
NG_033882.1:g.168880T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2405T>G	ENSP00000420082.2:p.Val802Gly
ENST00000470367.2:c.2693T>G	ENSP00000514541.1:p.Val898Gly
ENST00000483566.2:c.2405T>G	ENSP00000420252.2:p.Val802Gly
ENST00000699714.1:c.2405T>G	ENSP00000514539.1:p.Val802Gly
ENST00000699715.1:c.2405T>G	ENSP00000514540.1:p.Val802Gly
ENST00000699716.1:c.2405T>G	ENSP00000514542.1:p.Val802Gly
ENST00000699717.1:n.2131T>G
ENST00000699718.1:c.3803T>G	ENSP00000514543.1:p.Val1268Gly
ENST00000462833.6:c.3728T>G MANE Select	ENSP00000419361.1:p.Val1243Gly
ENST00000309879.9:c.2678T>G	ENSP00000308685.5:p.Val893Gly
ENST00000462833.5:c.3728T>G	ENSP00000419361.1:p.Val1243Gly
ENST00000478092.1:n.498T>G
ENST00000491190.5:c.2702T>G	ENSP00000418537.1:p.Val901Gly
NM_001199642.1:c.2678T>G	NP_001186571.1:p.Val893Gly
NM_183357.2:c.3728T>G	NP_899200.1:p.Val1243Gly
XM_005247077.2:c.3803T>G	XP_005247134.1:p.Val1268Gly
XM_005247078.1:c.2753T>G	XP_005247135.1:p.Val918Gly
XM_006713483.1:c.2702T>G	XP_006713546.1:p.Val901Gly
XM_006713484.1:c.2480T>G	XP_006713547.1:p.Val827Gly
XM_011512359.1:c.2804T>G	XP_011510661.1:p.Val935Gly
XM_011512360.1:c.2714T>G	XP_011510662.1:p.Val905Gly
XM_011512361.1:c.2480T>G	XP_011510663.1:p.Val827Gly
XM_005247077.4:c.3803T>G	XP_005247134.1:p.Val1268Gly
XM_011512359.2:c.2804T>G	XP_011510661.1:p.Val935Gly
XM_011512360.3:c.2714T>G	XP_011510662.1:p.Val905Gly
XM_017005638.1:c.2705T>G	XP_016861127.1:p.Val902Gly
XM_017005639.1:c.2705T>G	XP_016861128.1:p.Val902Gly
NM_001378259.1:c.3803T>G	NP_001365188.1:p.Val1268Gly
NM_183357.3:c.3728T>G MANE Select	NP_899200.1:p.Val1243Gly