Canonical Allele Identifier: CA2758207908

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123377994A>G , CM000665.2:g.123377994A>G	GRCh38
NC_000003.11:g.123096841A>G , CM000665.1:g.123096841A>G	GRCh37
NC_000003.10:g.124579531A>G	NCBI36
NG_033882.1:g.75552T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000466617.6:c.-189-25413T>C	ENSP00000420082.2:n.-189-25413T>C
ENST00000470367.2:c.100-25413T>C	ENSP00000514541.1:n.100-25413T>C
ENST00000483566.2:c.-189-25413T>C	ENSP00000420252.2:n.-189-25413T>C
ENST00000699714.1:c.-189-25413T>C	ENSP00000514539.1:n.-189-25413T>C
ENST00000699715.1:c.-189-25413T>C	ENSP00000514540.1:n.-189-25413T>C
ENST00000699716.1:c.-189-25413T>C	ENSP00000514542.1:n.-189-25413T>C
ENST00000699718.1:c.1135-25413T>C	ENSP00000514543.1:n.1135-25413T>C
ENST00000462833.6:c.1135-25413T>C MANE Select	ENSP00000419361.1:n.1135-25413T>C
ENST00000309879.9:c.85-25413T>C	ENSP00000308685.5:n.85-25413T>C
ENST00000462833.5:c.1135-25413T>C	ENSP00000419361.1:n.1135-25413T>C
ENST00000466617.5:c.-189-25413T>C	ENSP00000420082.1:n.-189-25413T>C
ENST00000470367.1:n.430-25413T>C
ENST00000476455.1:c.-109-9948T>C	ENSP00000417789.1:n.-109-9948T>C
ENST00000483566.1:c.-189-25413T>C	ENSP00000420252.1:n.-189-25413T>C
ENST00000491190.5:c.-109-9948T>C	ENSP00000418537.1:n.-109-9948T>C
NM_001199642.1:c.85-25413T>C	NP_001186571.1:n.85-25413T>C
NM_183357.2:c.1135-25413T>C	NP_899200.1:n.1135-25413T>C
XM_005247077.2:c.1135-25413T>C	XP_005247134.1:n.1135-25413T>C
XM_005247078.1:c.85-25413T>C	XP_005247135.1:n.85-25413T>C
XM_006713484.1:c.-189-25413T>C	XP_006713547.1:n.-189-25413T>C
XM_011512358.1:c.1135-25413T>C	XP_011510660.1:n.1135-25413T>C
XM_011512359.1:c.136-25413T>C	XP_011510661.1:n.136-25413T>C
XM_011512361.1:c.-189-25413T>C	XP_011510663.1:n.-189-25413T>C
XM_005247077.4:c.1135-25413T>C	XP_005247134.1:n.1135-25413T>C
XM_011512359.2:c.136-25413T>C	XP_011510661.1:n.136-25413T>C
XM_017005638.1:c.36+12347T>C	XP_016861127.1:n.36+12347T>C
XM_017005639.1:c.36+12801T>C	XP_016861128.1:n.36+12801T>C
NM_001378259.1:c.1135-25413T>C	NP_001365188.1:n.1135-25413T>C
NM_183357.3:c.1135-25413T>C MANE Select	NP_899200.1:n.1135-25413T>C