Canonical Allele Identifier: CA354223559

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123291222-A-G
• MyVariant Identifiers: chr3:g.123010069A>G (hg19) ; chr3:g.123291222A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123291222A>G , CM000665.2:g.123291222A>G	GRCh38
NC_000003.11:g.123010069A>G , CM000665.1:g.123010069A>G	GRCh37
NC_000003.10:g.124492759A>G	NCBI36
NG_033882.1:g.162324T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.1895T>C	ENSP00000420082.2:p.Met632Thr
ENST00000470367.2:c.2183T>C	ENSP00000514541.1:p.Met728Thr
ENST00000483566.2:c.1895T>C	ENSP00000420252.2:p.Met632Thr
ENST00000699714.1:c.1895T>C	ENSP00000514539.1:p.Met632Thr
ENST00000699715.1:c.1895T>C	ENSP00000514540.1:p.Met632Thr
ENST00000699716.1:c.1895T>C	ENSP00000514542.1:p.Met632Thr
ENST00000699717.1:n.1621T>C
ENST00000699718.1:c.3293T>C	ENSP00000514543.1:p.Met1098Thr
ENST00000462833.6:c.3218T>C MANE Select	ENSP00000419361.1:p.Met1073Thr
ENST00000309879.9:c.2168T>C	ENSP00000308685.5:p.Met723Thr
ENST00000462833.5:c.3218T>C	ENSP00000419361.1:p.Met1073Thr
ENST00000491190.5:c.2192T>C	ENSP00000418537.1:p.Met731Thr
NM_001199642.1:c.2168T>C	NP_001186571.1:p.Met723Thr
NM_183357.2:c.3218T>C	NP_899200.1:p.Met1073Thr
XM_005247077.2:c.3293T>C	XP_005247134.1:p.Met1098Thr
XM_005247078.1:c.2243T>C	XP_005247135.1:p.Met748Thr
XM_006713483.1:c.2192T>C	XP_006713546.1:p.Met731Thr
XM_006713484.1:c.1970T>C	XP_006713547.1:p.Met657Thr
XM_011512359.1:c.2294T>C	XP_011510661.1:p.Met765Thr
XM_011512360.1:c.2204T>C	XP_011510662.1:p.Met735Thr
XM_011512361.1:c.1970T>C	XP_011510663.1:p.Met657Thr
XM_005247077.4:c.3293T>C	XP_005247134.1:p.Met1098Thr
XM_011512359.2:c.2294T>C	XP_011510661.1:p.Met765Thr
XM_011512360.3:c.2204T>C	XP_011510662.1:p.Met735Thr
XM_017005638.1:c.2195T>C	XP_016861127.1:p.Met732Thr
XM_017005639.1:c.2195T>C	XP_016861128.1:p.Met732Thr
NM_001378259.1:c.3293T>C	NP_001365188.1:p.Met1098Thr
NM_183357.3:c.3218T>C MANE Select	NP_899200.1:p.Met1073Thr