Canonical Allele Identifier: CA435297661

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123284629-A-G
• MyVariant Identifiers: chr3:g.123003476A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284629A>G , CM000665.2:g.123284629A>G	GRCh38
NC_000003.11:g.123003476A>G , CM000665.1:g.123003476A>G	GRCh37
NC_000003.10:g.124486166A>G	NCBI36
NG_033882.1:g.168917T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2442T>C	ENSP00000420082.2:p.Asn814=
ENST00000470367.2:c.2730T>C	ENSP00000514541.1:p.Asn910=
ENST00000483566.2:c.2442T>C	ENSP00000420252.2:p.Asn814=
ENST00000699714.1:c.2442T>C	ENSP00000514539.1:p.Asn814=
ENST00000699715.1:c.2442T>C	ENSP00000514540.1:p.Asn814=
ENST00000699716.1:c.2442T>C	ENSP00000514542.1:p.Asn814=
ENST00000699717.1:n.2168T>C
ENST00000699718.1:c.3840T>C	ENSP00000514543.1:p.Asn1280=
ENST00000462833.6:c.3765T>C MANE Select	ENSP00000419361.1:p.Asn1255=
ENST00000309879.9:c.2715T>C	ENSP00000308685.5:p.Asn905=
ENST00000462833.5:c.3765T>C	ENSP00000419361.1:p.Asn1255=
ENST00000478092.1:n.535T>C
ENST00000491190.5:c.2739T>C	ENSP00000418537.1:p.Asn913=
NM_001199642.1:c.2715T>C	NP_001186571.1:p.Asn905=
NM_183357.2:c.3765T>C	NP_899200.1:p.Asn1255=
XM_005247077.2:c.3840T>C	XP_005247134.1:p.Asn1280=
XM_005247078.1:c.2790T>C	XP_005247135.1:p.Asn930=
XM_006713483.1:c.2739T>C	XP_006713546.1:p.Asn913=
XM_006713484.1:c.2517T>C	XP_006713547.1:p.Asn839=
XM_011512359.1:c.2841T>C	XP_011510661.1:p.Asn947=
XM_011512360.1:c.2751T>C	XP_011510662.1:p.Asn917=
XM_011512361.1:c.2517T>C	XP_011510663.1:p.Asn839=
XM_005247077.4:c.3840T>C	XP_005247134.1:p.Asn1280=
XM_011512359.2:c.2841T>C	XP_011510661.1:p.Asn947=
XM_011512360.3:c.2751T>C	XP_011510662.1:p.Asn917=
XM_017005638.1:c.2742T>C	XP_016861127.1:p.Asn914=
XM_017005639.1:c.2742T>C	XP_016861128.1:p.Asn914=
NM_001378259.1:c.3840T>C	NP_001365188.1:p.Asn1280=
NM_183357.3:c.3765T>C MANE Select	NP_899200.1:p.Asn1255=