Canonical Allele Identifier: CA346063767

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047359T>G (hg19) ; chr2:g.24824490T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824490T>G , CM000664.2:g.24824490T>G	GRCh38
NC_000002.11:g.25047359T>G , CM000664.1:g.25047359T>G	GRCh37
NC_000002.10:g.24900863T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2627A>C	ENSP00000384484.2:p.His876Pro
ENST00000679454.1:c.2624A>C MANE Select	ENSP00000505261.1:p.His875Pro
ENST00000260600.9:c.2624A>C	ENSP00000260600.5:p.His875Pro
ENST00000405392.5:c.2627A>C	ENSP00000384484.2:p.His876Pro
ENST00000606682.5:c.1565A>C	ENSP00000475652.1:p.His522Pro
NM_004036.3:c.2624A>C	NP_004027.2:p.His875Pro
XM_005264104.1:c.2627A>C	XP_005264161.1:p.His876Pro
XM_005264105.1:c.2624A>C	XP_005264162.1:p.His875Pro
XM_006711925.1:c.2693A>C	XP_006711988.1:p.His898Pro
XM_011532489.1:c.2750A>C	XP_011530791.1:p.His917Pro
XM_011532490.1:c.2747A>C	XP_011530792.1:p.His916Pro
XM_011532491.1:c.2684A>C	XP_011530793.1:p.His895Pro
XM_011532492.1:c.2750A>C	XP_011530794.1:p.His917Pro
XM_011532493.1:c.2612A>C	XP_011530795.1:p.His871Pro
XM_011532494.1:c.2552A>C	XP_011530796.1:p.His851Pro
XM_011532495.1:c.2084A>C	XP_011530797.1:p.His695Pro
XM_011532496.1:c.2027A>C	XP_011530798.1:p.His676Pro
NM_001320613.1:c.2627A>C	NP_001307542.1:p.His876Pro
NM_004036.4:c.2624A>C	NP_004027.2:p.His875Pro
XM_011532492.2:c.2750A>C	XP_011530794.1:p.His917Pro
XM_017003186.1:c.2690A>C	XP_016858675.1:p.His897Pro
XM_017003187.1:c.2681A>C	XP_016858676.1:p.His894Pro
XM_017003188.1:c.2747A>C	XP_016858677.1:p.His916Pro
XM_017003189.1:c.2609A>C	XP_016858678.1:p.His870Pro
XM_017003190.1:c.2486A>C	XP_016858679.1:p.His829Pro
XM_017003191.1:c.2114A>C	XP_016858680.1:p.His705Pro
XM_017003192.1:c.1904A>C	XP_016858681.1:p.His635Pro
XM_017003193.1:c.1901A>C	XP_016858682.1:p.His634Pro
NM_001320613.2:c.2627A>C	NP_001307542.1:p.His876Pro
NM_001377128.1:c.2690A>C	NP_001364057.1:p.His897Pro
NM_001377129.1:c.2486A>C	NP_001364058.1:p.His829Pro
NM_001377130.1:c.2219A>C	NP_001364059.1:p.His740Pro
NM_001377131.1:c.1901A>C	NP_001364060.1:p.His634Pro
NM_001377132.1:c.2624A>C	NP_001364061.1:p.His875Pro
NM_004036.5:c.2624A>C MANE Select	NP_004027.2:p.His875Pro