Canonical Allele Identifier: CA82899482

Gene: ADCY5

Linked Data

• dbSNP Id: rs1048578857
• gnomAD v2: 3-123003314-C-G
• gnomAD v3: 3-123284467-C-G
• gnomAD v4: 3-123284467-C-G
• MyVariant Identifiers: chr3:g.123003314C>G (hg19) ; chr3:g.123284467C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284467C>G , CM000665.2:g.123284467C>G	GRCh38
NC_000003.11:g.123003314C>G , CM000665.1:g.123003314C>G	GRCh37
NC_000003.10:g.124486004C>G	NCBI36
NG_033882.1:g.169079G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000466617.6:c.*141G>C	ENSP00000420082.2:n.*141G>C
ENST00000470367.2:c.*141G>C	ENSP00000514541.1:n.*141G>C
ENST00000483566.2:c.*141G>C	ENSP00000420252.2:n.*141G>C
ENST00000699714.1:c.*141G>C	ENSP00000514539.1:n.*141G>C
ENST00000699715.1:c.*141G>C	ENSP00000514540.1:n.*141G>C
ENST00000699716.1:c.*141G>C	ENSP00000514542.1:n.*141G>C
ENST00000699717.1:n.2330G>C
ENST00000699718.1:c.4002G>C	ENSP00000514543.1:n.4002G>C
ENST00000462833.6:c.*141G>C MANE Select	ENSP00000419361.1:n.*141G>C
ENST00000462833.5:c.*141G>C	ENSP00000419361.1:n.*141G>C
ENST00000478092.1:n.697G>C
ENST00000491190.5:c.*141G>C	ENSP00000418537.1:n.*141G>C
NM_001199642.1:c.*141G>C	NP_001186571.1:n.*141G>C
NM_183357.2:c.3927G>C	NP_899200.1:n.3927G>C
XM_005247077.2:c.*141G>C	XP_005247134.1:n.*141G>C
XM_005247078.1:c.*141G>C	XP_005247135.1:n.*141G>C
XM_006713483.1:c.*141G>C	XP_006713546.1:n.*141G>C
XM_006713484.1:c.*141G>C	XP_006713547.1:n.*141G>C
XM_011512359.1:c.*141G>C	XP_011510661.1:n.*141G>C
XM_011512360.1:c.*141G>C	XP_011510662.1:n.*141G>C
XM_011512361.1:c.*141G>C	XP_011510663.1:n.*141G>C
XM_005247077.4:c.*141G>C	XP_005247134.1:n.*141G>C
XM_011512359.2:c.*141G>C	XP_011510661.1:n.*141G>C
XM_011512360.3:c.*141G>C	XP_011510662.1:n.*141G>C
XM_017005638.1:c.*141G>C	XP_016861127.1:n.*141G>C
XM_017005639.1:c.*141G>C	XP_016861128.1:n.*141G>C
NM_001378259.1:c.*141G>C	NP_001365188.1:n.*141G>C
NM_183357.3:c.*141G>C MANE Select	NP_899200.1:n.*141G>C