Canonical Allele Identifier: CA1398327499

Gene: ADCY5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123284750_123284755delinsGGAGGA , CM000665.2:g.123284750_123284755delinsGGAGGA	GRCh38
NC_000003.11:g.123003597_123003602delinsGGAGGA , CM000665.1:g.123003597_123003602delinsGGAGGA	GRCh37
NC_000003.10:g.124486287_124486292delinsGGAGGA	NCBI36
NG_033882.1:g.168791_168796delinsTCCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000466617.6:c.2335-19_2335-14delinsTCCTCC	ENSP00000420082.2:n.2335-19_2335-14delinsTCCTCC
ENST00000470367.2:c.2623-19_2623-14delinsTCCTCC	ENSP00000514541.1:n.2623-19_2623-14delinsTCCTCC
ENST00000483566.2:c.2335-19_2335-14delinsTCCTCC	ENSP00000420252.2:n.2335-19_2335-14delinsTCCTCC
ENST00000699714.1:c.2335-19_2335-14delinsTCCTCC	ENSP00000514539.1:n.2335-19_2335-14delinsTCCTCC
ENST00000699715.1:c.2335-19_2335-14delinsTCCTCC	ENSP00000514540.1:n.2335-19_2335-14delinsTCCTCC
ENST00000699716.1:c.2335-19_2335-14delinsTCCTCC	ENSP00000514542.1:n.2335-19_2335-14delinsTCCTCC
ENST00000699717.1:n.2061-19_2061-14delinsTCCTCC
ENST00000699718.1:c.3733-19_3733-14delinsTCCTCC	ENSP00000514543.1:n.3733-19_3733-14delinsTCCTCC
ENST00000462833.6:c.3658-19_3658-14delinsTCCTCC MANE Select	ENSP00000419361.1:n.3658-19_3658-14delinsTCCTCC
ENST00000309879.9:c.2608-19_2608-14delinsTCCTCC	ENSP00000308685.5:n.2608-19_2608-14delinsTCCTCC
ENST00000462833.5:c.3658-19_3658-14delinsTCCTCC	ENSP00000419361.1:n.3658-19_3658-14delinsTCCTCC
ENST00000478092.1:n.428-19_428-14delinsTCCTCC
ENST00000491190.5:c.2632-19_2632-14delinsTCCTCC	ENSP00000418537.1:n.2632-19_2632-14delinsTCCTCC
NM_001199642.1:c.2608-19_2608-14delinsTCCTCC	NP_001186571.1:n.2608-19_2608-14delinsTCCTCC
NM_183357.2:c.3658-19_3658-14delinsTCCTCC	NP_899200.1:n.3658-19_3658-14delinsTCCTCC
XM_005247077.2:c.3733-19_3733-14delinsTCCTCC	XP_005247134.1:n.3733-19_3733-14delinsTCCTCC
XM_005247078.1:c.2683-19_2683-14delinsTCCTCC	XP_005247135.1:n.2683-19_2683-14delinsTCCTCC
XM_006713483.1:c.2632-19_2632-14delinsTCCTCC	XP_006713546.1:n.2632-19_2632-14delinsTCCTCC
XM_006713484.1:c.2410-19_2410-14delinsTCCTCC	XP_006713547.1:n.2410-19_2410-14delinsTCCTCC
XM_011512359.1:c.2734-19_2734-14delinsTCCTCC	XP_011510661.1:n.2734-19_2734-14delinsTCCTCC
XM_011512360.1:c.2644-19_2644-14delinsTCCTCC	XP_011510662.1:n.2644-19_2644-14delinsTCCTCC
XM_011512361.1:c.2410-19_2410-14delinsTCCTCC	XP_011510663.1:n.2410-19_2410-14delinsTCCTCC
XM_005247077.4:c.3733-19_3733-14delinsTCCTCC	XP_005247134.1:n.3733-19_3733-14delinsTCCTCC
XM_011512359.2:c.2734-19_2734-14delinsTCCTCC	XP_011510661.1:n.2734-19_2734-14delinsTCCTCC
XM_011512360.3:c.2644-19_2644-14delinsTCCTCC	XP_011510662.1:n.2644-19_2644-14delinsTCCTCC
XM_017005638.1:c.2635-19_2635-14delinsTCCTCC	XP_016861127.1:n.2635-19_2635-14delinsTCCTCC
XM_017005639.1:c.2635-19_2635-14delinsTCCTCC	XP_016861128.1:n.2635-19_2635-14delinsTCCTCC
NM_001378259.1:c.3733-19_3733-14delinsTCCTCC	NP_001365188.1:n.3733-19_3733-14delinsTCCTCC
NM_183357.3:c.3658-19_3658-14delinsTCCTCC MANE Select	NP_899200.1:n.3658-19_3658-14delinsTCCTCC