Canonical Allele Identifier: CA1398343336

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123319279_123319280delinsCG , CM000665.2:g.123319279_123319280delinsCG	GRCh38
NC_000003.11:g.123038126_123038127delinsCG , CM000665.1:g.123038126_123038127delinsCG	GRCh37
NC_000003.10:g.124520816_124520817delinsCG	NCBI36
NG_033882.1:g.134266_134267delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.933+394_933+395delinsCG	ENSP00000420082.2:n.933+394_933+395delinsCG
ENST00000470367.2:c.1221+394_1221+395delinsCG	ENSP00000514541.1:n.1221+394_1221+395delinsCG
ENST00000483566.2:c.933+394_933+395delinsCG	ENSP00000420252.2:n.933+394_933+395delinsCG
ENST00000699714.1:c.933+394_933+395delinsCG	ENSP00000514539.1:n.933+394_933+395delinsCG
ENST00000699715.1:c.933+394_933+395delinsCG	ENSP00000514540.1:n.933+394_933+395delinsCG
ENST00000699716.1:c.933+394_933+395delinsCG	ENSP00000514542.1:n.933+394_933+395delinsCG
ENST00000699718.1:c.2256+394_2256+395delinsCG	ENSP00000514543.1:n.2256+394_2256+395delinsCG
ENST00000699719.1:n.515+394_515+395delinsCG
ENST00000462833.6:c.2256+394_2256+395delinsCG MANE Select	ENSP00000419361.1:n.2256+394_2256+395delinsCG
ENST00000309879.9:c.1206+394_1206+395delinsCG	ENSP00000308685.5:n.1206+394_1206+395delinsCG
ENST00000462833.5:c.2256+394_2256+395delinsCG	ENSP00000419361.1:n.2256+394_2256+395delinsCG
ENST00000466617.5:c.933+394_933+395delinsCG	ENSP00000420082.1:n.933+394_933+395delinsCG
ENST00000491190.5:c.1155+394_1155+395delinsCG	ENSP00000418537.1:n.1155+394_1155+395delinsCG
NM_001199642.1:c.1206+394_1206+395delinsCG	NP_001186571.1:n.1206+394_1206+395delinsCG
NM_183357.2:c.2256+394_2256+395delinsCG	NP_899200.1:n.2256+394_2256+395delinsCG
XM_005247077.2:c.2256+394_2256+395delinsCG	XP_005247134.1:n.2256+394_2256+395delinsCG
XM_005247078.1:c.1206+394_1206+395delinsCG	XP_005247135.1:n.1206+394_1206+395delinsCG
XM_006713483.1:c.1155+394_1155+395delinsCG	XP_006713546.1:n.1155+394_1155+395delinsCG
XM_006713484.1:c.933+394_933+395delinsCG	XP_006713547.1:n.933+394_933+395delinsCG
XM_011512358.1:c.2256+394_2256+395delinsCG	XP_011510660.1:n.2256+394_2256+395delinsCG
XM_011512359.1:c.1257+394_1257+395delinsCG	XP_011510661.1:n.1257+394_1257+395delinsCG
XM_011512360.1:c.1167+394_1167+395delinsCG	XP_011510662.1:n.1167+394_1167+395delinsCG
XM_011512361.1:c.933+394_933+395delinsCG	XP_011510663.1:n.933+394_933+395delinsCG
XM_005247077.4:c.2256+394_2256+395delinsCG	XP_005247134.1:n.2256+394_2256+395delinsCG
XM_011512359.2:c.1257+394_1257+395delinsCG	XP_011510661.1:n.1257+394_1257+395delinsCG
XM_011512360.3:c.1167+394_1167+395delinsCG	XP_011510662.1:n.1167+394_1167+395delinsCG
XM_017005638.1:c.1158+394_1158+395delinsCG	XP_016861127.1:n.1158+394_1158+395delinsCG
XM_017005639.1:c.1158+394_1158+395delinsCG	XP_016861128.1:n.1158+394_1158+395delinsCG
NM_001378259.1:c.2256+394_2256+395delinsCG	NP_001365188.1:n.2256+394_2256+395delinsCG
NM_183357.3:c.2256+394_2256+395delinsCG MANE Select	NP_899200.1:n.2256+394_2256+395delinsCG