Canonical Allele Identifier: CA354222110

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123003549T>G (hg19) ; chr3:g.123284702T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284702T>G , CM000665.2:g.123284702T>G	GRCh38
NC_000003.11:g.123003549T>G , CM000665.1:g.123003549T>G	GRCh37
NC_000003.10:g.124486239T>G	NCBI36
NG_033882.1:g.168844A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2369A>C	ENSP00000420082.2:p.Asn790Thr
ENST00000470367.2:c.2657A>C	ENSP00000514541.1:p.Asn886Thr
ENST00000483566.2:c.2369A>C	ENSP00000420252.2:p.Asn790Thr
ENST00000699714.1:c.2369A>C	ENSP00000514539.1:p.Asn790Thr
ENST00000699715.1:c.2369A>C	ENSP00000514540.1:p.Asn790Thr
ENST00000699716.1:c.2369A>C	ENSP00000514542.1:p.Asn790Thr
ENST00000699717.1:n.2095A>C
ENST00000699718.1:c.3767A>C	ENSP00000514543.1:p.Asn1256Thr
ENST00000462833.6:c.3692A>C MANE Select	ENSP00000419361.1:p.Asn1231Thr
ENST00000309879.9:c.2642A>C	ENSP00000308685.5:p.Asn881Thr
ENST00000462833.5:c.3692A>C	ENSP00000419361.1:p.Asn1231Thr
ENST00000478092.1:n.462A>C
ENST00000491190.5:c.2666A>C	ENSP00000418537.1:p.Asn889Thr
NM_001199642.1:c.2642A>C	NP_001186571.1:p.Asn881Thr
NM_183357.2:c.3692A>C	NP_899200.1:p.Asn1231Thr
XM_005247077.2:c.3767A>C	XP_005247134.1:p.Asn1256Thr
XM_005247078.1:c.2717A>C	XP_005247135.1:p.Asn906Thr
XM_006713483.1:c.2666A>C	XP_006713546.1:p.Asn889Thr
XM_006713484.1:c.2444A>C	XP_006713547.1:p.Asn815Thr
XM_011512359.1:c.2768A>C	XP_011510661.1:p.Asn923Thr
XM_011512360.1:c.2678A>C	XP_011510662.1:p.Asn893Thr
XM_011512361.1:c.2444A>C	XP_011510663.1:p.Asn815Thr
XM_005247077.4:c.3767A>C	XP_005247134.1:p.Asn1256Thr
XM_011512359.2:c.2768A>C	XP_011510661.1:p.Asn923Thr
XM_011512360.3:c.2678A>C	XP_011510662.1:p.Asn893Thr
XM_017005638.1:c.2669A>C	XP_016861127.1:p.Asn890Thr
XM_017005639.1:c.2669A>C	XP_016861128.1:p.Asn890Thr
NM_001378259.1:c.3767A>C	NP_001365188.1:p.Asn1256Thr
NM_183357.3:c.3692A>C MANE Select	NP_899200.1:p.Asn1231Thr