Canonical Allele Identifier: CA435431420

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123291263-A-G
• MyVariant Identifiers: chr3:g.123010110A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291263A>G , CM000665.2:g.123291263A>G	GRCh38
NC_000003.11:g.123010110A>G , CM000665.1:g.123010110A>G	GRCh37
NC_000003.10:g.124492800A>G	NCBI36
NG_033882.1:g.162283T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000466617.6:c.1854T>C	ENSP00000420082.2:p.Asn618=
ENST00000470367.2:c.2142T>C	ENSP00000514541.1:p.Asn714=
ENST00000483566.2:c.1854T>C	ENSP00000420252.2:p.Asn618=
ENST00000699714.1:c.1854T>C	ENSP00000514539.1:p.Asn618=
ENST00000699715.1:c.1854T>C	ENSP00000514540.1:p.Asn618=
ENST00000699716.1:c.1854T>C	ENSP00000514542.1:p.Asn618=
ENST00000699717.1:n.1580T>C
ENST00000699718.1:c.3252T>C	ENSP00000514543.1:p.Asn1084=
ENST00000462833.6:c.3177T>C MANE Select	ENSP00000419361.1:p.Asn1059=
ENST00000309879.9:c.2127T>C	ENSP00000308685.5:p.Asn709=
ENST00000462833.5:c.3177T>C	ENSP00000419361.1:p.Asn1059=
ENST00000491190.5:c.2151T>C	ENSP00000418537.1:p.Asn717=
NM_001199642.1:c.2127T>C	NP_001186571.1:p.Asn709=
NM_183357.2:c.3177T>C	NP_899200.1:p.Asn1059=
XM_005247077.2:c.3252T>C	XP_005247134.1:p.Asn1084=
XM_005247078.1:c.2202T>C	XP_005247135.1:p.Asn734=
XM_006713483.1:c.2151T>C	XP_006713546.1:p.Asn717=
XM_006713484.1:c.1929T>C	XP_006713547.1:p.Asn643=
XM_011512359.1:c.2253T>C	XP_011510661.1:p.Asn751=
XM_011512360.1:c.2163T>C	XP_011510662.1:p.Asn721=
XM_011512361.1:c.1929T>C	XP_011510663.1:p.Asn643=
XM_005247077.4:c.3252T>C	XP_005247134.1:p.Asn1084=
XM_011512359.2:c.2253T>C	XP_011510661.1:p.Asn751=
XM_011512360.3:c.2163T>C	XP_011510662.1:p.Asn721=
XM_017005638.1:c.2154T>C	XP_016861127.1:p.Asn718=
XM_017005639.1:c.2154T>C	XP_016861128.1:p.Asn718=
NM_001378259.1:c.3252T>C	NP_001365188.1:p.Asn1084=
NM_183357.3:c.3177T>C MANE Select	NP_899200.1:p.Asn1059=