Canonical Allele Identifier: CA1239072888

Gene: ADCY3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824349_24824350delinsTG , CM000664.2:g.24824349_24824350delinsTG	GRCh38
NC_000002.11:g.25047218_25047219delinsTG , CM000664.1:g.25047218_25047219delinsTG	GRCh37
NC_000002.10:g.24900722_24900723delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2739+28_2739+29delinsCA	ENSP00000384484.2:n.2739+28_2739+29delinsCA
ENST00000679454.1:c.2736+28_2736+29delinsCA MANE Select	ENSP00000505261.1:n.2736+28_2736+29delinsCA
ENST00000260600.9:c.2736+28_2736+29delinsCA	ENSP00000260600.5:n.2736+28_2736+29delinsCA
ENST00000405392.5:c.2739+28_2739+29delinsCA	ENSP00000384484.2:n.2739+28_2739+29delinsCA
ENST00000606682.5:c.1677+28_1677+29delinsCA	ENSP00000475652.1:n.1677+28_1677+29delinsCA
NM_004036.3:c.2736+28_2736+29delinsCA	NP_004027.2:n.2736+28_2736+29delinsCA
XM_005264104.1:c.2739+28_2739+29delinsCA	XP_005264161.1:n.2739+28_2739+29delinsCA
XM_005264105.1:c.2736+28_2736+29delinsCA	XP_005264162.1:n.2736+28_2736+29delinsCA
XM_006711925.1:c.2805+28_2805+29delinsCA	XP_006711988.1:n.2805+28_2805+29delinsCA
XM_011532489.1:c.2862+28_2862+29delinsCA	XP_011530791.1:n.2862+28_2862+29delinsCA
XM_011532490.1:c.2859+28_2859+29delinsCA	XP_011530792.1:n.2859+28_2859+29delinsCA
XM_011532491.1:c.2796+28_2796+29delinsCA	XP_011530793.1:n.2796+28_2796+29delinsCA
XM_011532492.1:c.2862+28_2862+29delinsCA	XP_011530794.1:n.2862+28_2862+29delinsCA
XM_011532493.1:c.2724+28_2724+29delinsCA	XP_011530795.1:n.2724+28_2724+29delinsCA
XM_011532494.1:c.2664+28_2664+29delinsCA	XP_011530796.1:n.2664+28_2664+29delinsCA
XM_011532495.1:c.2196+28_2196+29delinsCA	XP_011530797.1:n.2196+28_2196+29delinsCA
XM_011532496.1:c.2139+28_2139+29delinsCA	XP_011530798.1:n.2139+28_2139+29delinsCA
NM_001320613.1:c.2739+28_2739+29delinsCA	NP_001307542.1:n.2739+28_2739+29delinsCA
NM_004036.4:c.2736+28_2736+29delinsCA	NP_004027.2:n.2736+28_2736+29delinsCA
XM_011532492.2:c.2862+28_2862+29delinsCA	XP_011530794.1:n.2862+28_2862+29delinsCA
XM_017003186.1:c.2802+28_2802+29delinsCA	XP_016858675.1:n.2802+28_2802+29delinsCA
XM_017003187.1:c.2793+28_2793+29delinsCA	XP_016858676.1:n.2793+28_2793+29delinsCA
XM_017003188.1:c.2859+28_2859+29delinsCA	XP_016858677.1:n.2859+28_2859+29delinsCA
XM_017003189.1:c.2721+28_2721+29delinsCA	XP_016858678.1:n.2721+28_2721+29delinsCA
XM_017003190.1:c.2598+28_2598+29delinsCA	XP_016858679.1:n.2598+28_2598+29delinsCA
XM_017003191.1:c.2226+28_2226+29delinsCA	XP_016858680.1:n.2226+28_2226+29delinsCA
XM_017003192.1:c.2016+28_2016+29delinsCA	XP_016858681.1:n.2016+28_2016+29delinsCA
XM_017003193.1:c.2013+28_2013+29delinsCA	XP_016858682.1:n.2013+28_2013+29delinsCA
NM_001320613.2:c.2739+28_2739+29delinsCA	NP_001307542.1:n.2739+28_2739+29delinsCA
NM_001377128.1:c.2802+28_2802+29delinsCA	NP_001364057.1:n.2802+28_2802+29delinsCA
NM_001377129.1:c.2598+28_2598+29delinsCA	NP_001364058.1:n.2598+28_2598+29delinsCA
NM_001377130.1:c.2331+28_2331+29delinsCA	NP_001364059.1:n.2331+28_2331+29delinsCA
NM_001377131.1:c.2013+28_2013+29delinsCA	NP_001364060.1:n.2013+28_2013+29delinsCA
NM_001377132.1:c.2736+28_2736+29delinsCA	NP_001364061.1:n.2736+28_2736+29delinsCA
NM_004036.5:c.2736+28_2736+29delinsCA MANE Select	NP_004027.2:n.2736+28_2736+29delinsCA