Canonical Allele Identifier: CA346063301

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047246C>A (hg19) ; chr2:g.24824377C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824377C>A , CM000664.2:g.24824377C>A	GRCh38
NC_000002.11:g.25047246C>A , CM000664.1:g.25047246C>A	GRCh37
NC_000002.10:g.24900750C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2739+1G>T	ENSP00000384484.2:n.2739+1G>T
ENST00000679454.1:c.2736+1G>T MANE Select	ENSP00000505261.1:n.2736+1G>T
ENST00000260600.9:c.2736+1G>T	ENSP00000260600.5:n.2736+1G>T
ENST00000405392.5:c.2739+1G>T	ENSP00000384484.2:n.2739+1G>T
ENST00000606682.5:c.1677+1G>T	ENSP00000475652.1:n.1677+1G>T
NM_004036.3:c.2736+1G>T	NP_004027.2:n.2736+1G>T
XM_005264104.1:c.2739+1G>T	XP_005264161.1:n.2739+1G>T
XM_005264105.1:c.2736+1G>T	XP_005264162.1:n.2736+1G>T
XM_006711925.1:c.2805+1G>T	XP_006711988.1:n.2805+1G>T
XM_011532489.1:c.2862+1G>T	XP_011530791.1:n.2862+1G>T
XM_011532490.1:c.2859+1G>T	XP_011530792.1:n.2859+1G>T
XM_011532491.1:c.2796+1G>T	XP_011530793.1:n.2796+1G>T
XM_011532492.1:c.2862+1G>T	XP_011530794.1:n.2862+1G>T
XM_011532493.1:c.2724+1G>T	XP_011530795.1:n.2724+1G>T
XM_011532494.1:c.2664+1G>T	XP_011530796.1:n.2664+1G>T
XM_011532495.1:c.2196+1G>T	XP_011530797.1:n.2196+1G>T
XM_011532496.1:c.2139+1G>T	XP_011530798.1:n.2139+1G>T
NM_001320613.1:c.2739+1G>T	NP_001307542.1:n.2739+1G>T
NM_004036.4:c.2736+1G>T	NP_004027.2:n.2736+1G>T
XM_011532492.2:c.2862+1G>T	XP_011530794.1:n.2862+1G>T
XM_017003186.1:c.2802+1G>T	XP_016858675.1:n.2802+1G>T
XM_017003187.1:c.2793+1G>T	XP_016858676.1:n.2793+1G>T
XM_017003188.1:c.2859+1G>T	XP_016858677.1:n.2859+1G>T
XM_017003189.1:c.2721+1G>T	XP_016858678.1:n.2721+1G>T
XM_017003190.1:c.2598+1G>T	XP_016858679.1:n.2598+1G>T
XM_017003191.1:c.2226+1G>T	XP_016858680.1:n.2226+1G>T
XM_017003192.1:c.2016+1G>T	XP_016858681.1:n.2016+1G>T
XM_017003193.1:c.2013+1G>T	XP_016858682.1:n.2013+1G>T
NM_001320613.2:c.2739+1G>T	NP_001307542.1:n.2739+1G>T
NM_001377128.1:c.2802+1G>T	NP_001364057.1:n.2802+1G>T
NM_001377129.1:c.2598+1G>T	NP_001364058.1:n.2598+1G>T
NM_001377130.1:c.2331+1G>T	NP_001364059.1:n.2331+1G>T
NM_001377131.1:c.2013+1G>T	NP_001364060.1:n.2013+1G>T
NM_001377132.1:c.2736+1G>T	NP_001364061.1:n.2736+1G>T
NM_004036.5:c.2736+1G>T MANE Select	NP_004027.2:n.2736+1G>T