Canonical Allele Identifier: CA2667293777

Gene: ADCY5

Linked Data

• gnomAD v4: 3-123325614-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123325614C>A , CM000665.2:g.123325614C>A	GRCh38
NC_000003.11:g.123044461C>A , CM000665.1:g.123044461C>A	GRCh37
NC_000003.10:g.124527151C>A	NCBI36
NG_033882.1:g.127932G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.625-152G>T	ENSP00000420082.2:n.625-152G>T
ENST00000470367.2:c.913-152G>T	ENSP00000514541.1:n.913-152G>T
ENST00000483566.2:c.625-152G>T	ENSP00000420252.2:n.625-152G>T
ENST00000699714.1:c.625-152G>T	ENSP00000514539.1:n.625-152G>T
ENST00000699715.1:c.625-152G>T	ENSP00000514540.1:n.625-152G>T
ENST00000699716.1:c.625-152G>T	ENSP00000514542.1:n.625-152G>T
ENST00000699718.1:c.1948-152G>T	ENSP00000514543.1:n.1948-152G>T
ENST00000699719.1:n.207-152G>T
ENST00000462833.6:c.1948-152G>T MANE Select	ENSP00000419361.1:n.1948-152G>T
ENST00000309879.9:c.898-152G>T	ENSP00000308685.5:n.898-152G>T
ENST00000462833.5:c.1948-152G>T	ENSP00000419361.1:n.1948-152G>T
ENST00000466617.5:c.625-152G>T	ENSP00000420082.1:n.625-152G>T
ENST00000491190.5:c.847-152G>T	ENSP00000418537.1:n.847-152G>T
NM_001199642.1:c.898-152G>T	NP_001186571.1:n.898-152G>T
NM_183357.2:c.1948-152G>T	NP_899200.1:n.1948-152G>T
XM_005247077.2:c.1948-152G>T	XP_005247134.1:n.1948-152G>T
XM_005247078.1:c.898-152G>T	XP_005247135.1:n.898-152G>T
XM_006713483.1:c.847-152G>T	XP_006713546.1:n.847-152G>T
XM_006713484.1:c.625-152G>T	XP_006713547.1:n.625-152G>T
XM_011512358.1:c.1948-152G>T	XP_011510660.1:n.1948-152G>T
XM_011512359.1:c.949-152G>T	XP_011510661.1:n.949-152G>T
XM_011512360.1:c.859-152G>T	XP_011510662.1:n.859-152G>T
XM_011512361.1:c.625-152G>T	XP_011510663.1:n.625-152G>T
XM_005247077.4:c.1948-152G>T	XP_005247134.1:n.1948-152G>T
XM_011512359.2:c.949-152G>T	XP_011510661.1:n.949-152G>T
XM_011512360.3:c.859-152G>T	XP_011510662.1:n.859-152G>T
XM_017005638.1:c.850-152G>T	XP_016861127.1:n.850-152G>T
XM_017005639.1:c.850-152G>T	XP_016861128.1:n.850-152G>T
NM_001378259.1:c.1948-152G>T	NP_001365188.1:n.1948-152G>T
NM_183357.3:c.1948-152G>T MANE Select	NP_899200.1:n.1948-152G>T