Canonical Allele Identifier: CA1553644

Gene: ADCY3

Linked Data

• dbSNP Id: rs769983667
• ExAC: 2:25047243 T / TCA
• gnomAD v2: 2-25047243-T-TCA
• gnomAD v3: 2-24824374-T-TCA
• gnomAD v4: 2-24824374-T-TCA
• MyVariant Identifiers: chr2:g.25047243_25047244insCA (hg19) ; chr2:g.24824374_24824375insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824376_24824377dup , CM000664.2:g.24824376_24824377dup	GRCh38
NC_000002.11:g.25047245_25047246dup , CM000664.1:g.25047245_25047246dup	GRCh37
NC_000002.10:g.24900749_24900750dup	NCBI36

Transcript Alleles

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