Canonical Allele Identifier: CA354222525

Gene: ADCY5

Linked Data

• MyVariant Identifiers: chr3:g.123071298T>G (hg19) ; chr3:g.123352451T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123352451T>G , CM000665.2:g.123352451T>G	GRCh38
NC_000003.11:g.123071298T>G , CM000665.1:g.123071298T>G	GRCh37
NC_000003.10:g.124553988T>G	NCBI36
NG_033882.1:g.101095A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.-59A>C	ENSP00000420082.2:n.-59A>C
ENST00000470367.2:c.230A>C	ENSP00000514541.1:p.Gln77Pro
ENST00000483566.2:c.-59A>C	ENSP00000420252.2:n.-59A>C
ENST00000699714.1:c.-59A>C	ENSP00000514539.1:n.-59A>C
ENST00000699715.1:c.-59A>C	ENSP00000514540.1:n.-59A>C
ENST00000699716.1:c.-59A>C	ENSP00000514542.1:n.-59A>C
ENST00000699718.1:c.1265A>C	ENSP00000514543.1:p.Gln422Pro
ENST00000462833.6:c.1265A>C MANE Select	ENSP00000419361.1:p.Gln422Pro
ENST00000309879.9:c.215A>C	ENSP00000308685.5:p.Gln72Pro
ENST00000462833.5:c.1265A>C	ENSP00000419361.1:p.Gln422Pro
ENST00000466617.5:c.-59A>C	ENSP00000420082.1:n.-59A>C
ENST00000470367.1:n.560A>C
ENST00000476455.1:c.169A>C	ENSP00000417789.1:p.Ser57Arg
ENST00000483566.1:c.-59A>C	ENSP00000420252.1:n.-59A>C
ENST00000491190.5:c.164A>C	ENSP00000418537.1:p.Gln55Pro
NM_001199642.1:c.215A>C	NP_001186571.1:p.Gln72Pro
NM_183357.2:c.1265A>C	NP_899200.1:p.Gln422Pro
XM_005247077.2:c.1265A>C	XP_005247134.1:p.Gln422Pro
XM_005247078.1:c.215A>C	XP_005247135.1:p.Gln72Pro
XM_006713483.1:c.164A>C	XP_006713546.1:p.Gln55Pro
XM_006713484.1:c.-59A>C	XP_006713547.1:n.-59A>C
XM_011512358.1:c.1265A>C	XP_011510660.1:p.Gln422Pro
XM_011512359.1:c.266A>C	XP_011510661.1:p.Gln89Pro
XM_011512360.1:c.176A>C	XP_011510662.1:p.Gln59Pro
XM_011512361.1:c.-59A>C	XP_011510663.1:n.-59A>C
XM_005247077.4:c.1265A>C	XP_005247134.1:p.Gln422Pro
XM_011512359.2:c.266A>C	XP_011510661.1:p.Gln89Pro
XM_011512360.3:c.176A>C	XP_011510662.1:p.Gln59Pro
XM_017005638.1:c.167A>C	XP_016861127.1:p.Gln56Pro
XM_017005639.1:c.167A>C	XP_016861128.1:p.Gln56Pro
NM_001378259.1:c.1265A>C	NP_001365188.1:p.Gln422Pro
NM_183357.3:c.1265A>C MANE Select	NP_899200.1:p.Gln422Pro