Canonical Allele Identifier: CA82914325

Gene: ADCY5

Linked Data

• dbSNP Id: rs889328564
• gnomAD v2: 3-123065781-C-G
• gnomAD v3: 3-123346934-C-G
• gnomAD v4: 3-123346934-C-G
• MyVariant Identifiers: chr3:g.123065781C>G (hg19) ; chr3:g.123346934C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123346934C>G , CM000665.2:g.123346934C>G	GRCh38
NC_000003.11:g.123065781C>G , CM000665.1:g.123065781C>G	GRCh37
NC_000003.10:g.124548471C>G	NCBI36
NG_033882.1:g.106612G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000466617.6:c.83+848G>C	ENSP00000420082.2:n.83+848G>C
ENST00000470367.2:c.371+848G>C	ENSP00000514541.1:n.371+848G>C
ENST00000483566.2:c.83+848G>C	ENSP00000420252.2:n.83+848G>C
ENST00000699714.1:c.83+848G>C	ENSP00000514539.1:n.83+848G>C
ENST00000699715.1:c.83+848G>C	ENSP00000514540.1:n.83+848G>C
ENST00000699716.1:c.83+848G>C	ENSP00000514542.1:n.83+848G>C
ENST00000699718.1:c.1406+848G>C	ENSP00000514543.1:n.1406+848G>C
ENST00000462833.6:c.1406+848G>C MANE Select	ENSP00000419361.1:n.1406+848G>C
ENST00000309879.9:c.356+848G>C	ENSP00000308685.5:n.356+848G>C
ENST00000462833.5:c.1406+848G>C	ENSP00000419361.1:n.1406+848G>C
ENST00000466617.5:c.83+848G>C	ENSP00000420082.1:n.83+848G>C
ENST00000476455.1:c.*73+848G>C	ENSP00000417789.1:n.*73+848G>C
ENST00000483566.1:c.83+848G>C	ENSP00000420252.1:n.83+848G>C
ENST00000491190.5:c.305+848G>C	ENSP00000418537.1:n.305+848G>C
NM_001199642.1:c.356+848G>C	NP_001186571.1:n.356+848G>C
NM_183357.2:c.1406+848G>C	NP_899200.1:n.1406+848G>C
XM_005247077.2:c.1406+848G>C	XP_005247134.1:n.1406+848G>C
XM_005247078.1:c.356+848G>C	XP_005247135.1:n.356+848G>C
XM_006713483.1:c.305+848G>C	XP_006713546.1:n.305+848G>C
XM_006713484.1:c.83+848G>C	XP_006713547.1:n.83+848G>C
XM_011512358.1:c.1406+848G>C	XP_011510660.1:n.1406+848G>C
XM_011512359.1:c.407+848G>C	XP_011510661.1:n.407+848G>C
XM_011512360.1:c.317+848G>C	XP_011510662.1:n.317+848G>C
XM_011512361.1:c.83+848G>C	XP_011510663.1:n.83+848G>C
XM_005247077.4:c.1406+848G>C	XP_005247134.1:n.1406+848G>C
XM_011512359.2:c.407+848G>C	XP_011510661.1:n.407+848G>C
XM_011512360.3:c.317+848G>C	XP_011510662.1:n.317+848G>C
XM_017005638.1:c.308+848G>C	XP_016861127.1:n.308+848G>C
XM_017005639.1:c.308+848G>C	XP_016861128.1:n.308+848G>C
NM_001378259.1:c.1406+848G>C	NP_001365188.1:n.1406+848G>C
NM_183357.3:c.1406+848G>C MANE Select	NP_899200.1:n.1406+848G>C