Canonical Allele Identifier: CA354222010

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003522A>C (hg19) ; chr3:g.123284675A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284675A>C , CM000665.2:g.123284675A>C	GRCh38
NC_000003.11:g.123003522A>C , CM000665.1:g.123003522A>C	GRCh37
NC_000003.10:g.124486212A>C	NCBI36
NG_033882.1:g.168871T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2396T>G	ENSP00000420082.2:p.Val799Gly
ENST00000470367.2:c.2684T>G	ENSP00000514541.1:p.Val895Gly
ENST00000483566.2:c.2396T>G	ENSP00000420252.2:p.Val799Gly
ENST00000699714.1:c.2396T>G	ENSP00000514539.1:p.Val799Gly
ENST00000699715.1:c.2396T>G	ENSP00000514540.1:p.Val799Gly
ENST00000699716.1:c.2396T>G	ENSP00000514542.1:p.Val799Gly
ENST00000699717.1:n.2122T>G
ENST00000699718.1:c.3794T>G	ENSP00000514543.1:p.Val1265Gly
ENST00000462833.6:c.3719T>G MANE Select	ENSP00000419361.1:p.Val1240Gly
ENST00000309879.9:c.2669T>G	ENSP00000308685.5:p.Val890Gly
ENST00000462833.5:c.3719T>G	ENSP00000419361.1:p.Val1240Gly
ENST00000478092.1:n.489T>G
ENST00000491190.5:c.2693T>G	ENSP00000418537.1:p.Val898Gly
NM_001199642.1:c.2669T>G	NP_001186571.1:p.Val890Gly
NM_183357.2:c.3719T>G	NP_899200.1:p.Val1240Gly
XM_005247077.2:c.3794T>G	XP_005247134.1:p.Val1265Gly
XM_005247078.1:c.2744T>G	XP_005247135.1:p.Val915Gly
XM_006713483.1:c.2693T>G	XP_006713546.1:p.Val898Gly
XM_006713484.1:c.2471T>G	XP_006713547.1:p.Val824Gly
XM_011512359.1:c.2795T>G	XP_011510661.1:p.Val932Gly
XM_011512360.1:c.2705T>G	XP_011510662.1:p.Val902Gly
XM_011512361.1:c.2471T>G	XP_011510663.1:p.Val824Gly
XM_005247077.4:c.3794T>G	XP_005247134.1:p.Val1265Gly
XM_011512359.2:c.2795T>G	XP_011510661.1:p.Val932Gly
XM_011512360.3:c.2705T>G	XP_011510662.1:p.Val902Gly
XM_017005638.1:c.2696T>G	XP_016861127.1:p.Val899Gly
XM_017005639.1:c.2696T>G	XP_016861128.1:p.Val899Gly
NM_001378259.1:c.3794T>G	NP_001365188.1:p.Val1265Gly
NM_183357.3:c.3719T>G MANE Select	NP_899200.1:p.Val1240Gly