Canonical Allele Identifier: CA2576824

Gene: ADCY5

Linked Data

• dbSNP Id: rs750807988
• ExAC: 3:123010055 C / A
• gnomAD v2: 3-123010055-C-A
• gnomAD v4: 3-123291208-C-A
• MyVariant Identifiers: chr3:g.123010055C>A (hg19) ; chr3:g.123291208C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291208C>A , CM000665.2:g.123291208C>A	GRCh38
NC_000003.11:g.123010055C>A , CM000665.1:g.123010055C>A	GRCh37
NC_000003.10:g.124492745C>A	NCBI36
NG_033882.1:g.162338G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1909G>T	ENSP00000420082.2:p.Ala637Ser
ENST00000470367.2:c.2197G>T	ENSP00000514541.1:p.Ala733Ser
ENST00000483566.2:c.1909G>T	ENSP00000420252.2:p.Ala637Ser
ENST00000699714.1:c.1909G>T	ENSP00000514539.1:p.Ala637Ser
ENST00000699715.1:c.1909G>T	ENSP00000514540.1:p.Ala637Ser
ENST00000699716.1:c.1909G>T	ENSP00000514542.1:p.Ala637Ser
ENST00000699717.1:n.1635G>T
ENST00000699718.1:c.3307G>T	ENSP00000514543.1:p.Ala1103Ser
ENST00000462833.6:c.3232G>T MANE Select	ENSP00000419361.1:p.Ala1078Ser
ENST00000309879.9:c.2182G>T	ENSP00000308685.5:p.Ala728Ser
ENST00000462833.5:c.3232G>T	ENSP00000419361.1:p.Ala1078Ser
ENST00000491190.5:c.2206G>T	ENSP00000418537.1:p.Ala736Ser
NM_001199642.1:c.2182G>T	NP_001186571.1:p.Ala728Ser
NM_183357.2:c.3232G>T	NP_899200.1:p.Ala1078Ser
XM_005247077.2:c.3307G>T	XP_005247134.1:p.Ala1103Ser
XM_005247078.1:c.2257G>T	XP_005247135.1:p.Ala753Ser
XM_006713483.1:c.2206G>T	XP_006713546.1:p.Ala736Ser
XM_006713484.1:c.1984G>T	XP_006713547.1:p.Ala662Ser
XM_011512359.1:c.2308G>T	XP_011510661.1:p.Ala770Ser
XM_011512360.1:c.2218G>T	XP_011510662.1:p.Ala740Ser
XM_011512361.1:c.1984G>T	XP_011510663.1:p.Ala662Ser
XM_005247077.4:c.3307G>T	XP_005247134.1:p.Ala1103Ser
XM_011512359.2:c.2308G>T	XP_011510661.1:p.Ala770Ser
XM_011512360.3:c.2218G>T	XP_011510662.1:p.Ala740Ser
XM_017005638.1:c.2209G>T	XP_016861127.1:p.Ala737Ser
XM_017005639.1:c.2209G>T	XP_016861128.1:p.Ala737Ser
NM_001378259.1:c.3307G>T	NP_001365188.1:p.Ala1103Ser
NM_183357.3:c.3232G>T MANE Select	NP_899200.1:p.Ala1078Ser