Canonical Allele Identifier: CA354223399

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123009998G>T (hg19) ; chr3:g.123291151G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291151G>T , CM000665.2:g.123291151G>T	GRCh38
NC_000003.11:g.123009998G>T , CM000665.1:g.123009998G>T	GRCh37
NC_000003.10:g.124492688G>T	NCBI36
NG_033882.1:g.162395C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1966C>A	ENSP00000420082.2:p.Leu656Met
ENST00000470367.2:c.2254C>A	ENSP00000514541.1:p.Leu752Met
ENST00000483566.2:c.1966C>A	ENSP00000420252.2:p.Leu656Met
ENST00000699714.1:c.1966C>A	ENSP00000514539.1:p.Leu656Met
ENST00000699715.1:c.1966C>A	ENSP00000514540.1:p.Leu656Met
ENST00000699716.1:c.1966C>A	ENSP00000514542.1:p.Leu656Met
ENST00000699717.1:n.1692C>A
ENST00000699718.1:c.3364C>A	ENSP00000514543.1:p.Leu1122Met
ENST00000462833.6:c.3289C>A MANE Select	ENSP00000419361.1:p.Leu1097Met
ENST00000309879.9:c.2239C>A	ENSP00000308685.5:p.Leu747Met
ENST00000462833.5:c.3289C>A	ENSP00000419361.1:p.Leu1097Met
ENST00000491190.5:c.2263C>A	ENSP00000418537.1:p.Leu755Met
NM_001199642.1:c.2239C>A	NP_001186571.1:p.Leu747Met
NM_183357.2:c.3289C>A	NP_899200.1:p.Leu1097Met
XM_005247077.2:c.3364C>A	XP_005247134.1:p.Leu1122Met
XM_005247078.1:c.2314C>A	XP_005247135.1:p.Leu772Met
XM_006713483.1:c.2263C>A	XP_006713546.1:p.Leu755Met
XM_006713484.1:c.2041C>A	XP_006713547.1:p.Leu681Met
XM_011512359.1:c.2365C>A	XP_011510661.1:p.Leu789Met
XM_011512360.1:c.2275C>A	XP_011510662.1:p.Leu759Met
XM_011512361.1:c.2041C>A	XP_011510663.1:p.Leu681Met
XM_005247077.4:c.3364C>A	XP_005247134.1:p.Leu1122Met
XM_011512359.2:c.2365C>A	XP_011510661.1:p.Leu789Met
XM_011512360.3:c.2275C>A	XP_011510662.1:p.Leu759Met
XM_017005638.1:c.2266C>A	XP_016861127.1:p.Leu756Met
XM_017005639.1:c.2266C>A	XP_016861128.1:p.Leu756Met
NM_001378259.1:c.3364C>A	NP_001365188.1:p.Leu1122Met
NM_183357.3:c.3289C>A MANE Select	NP_899200.1:p.Leu1097Met