Canonical Allele Identifier: CA346063475

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25047282C>A (hg19) ; chr2:g.24824413C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824413C>A , CM000664.2:g.24824413C>A	GRCh38
NC_000002.11:g.25047282C>A , CM000664.1:g.25047282C>A	GRCh37
NC_000002.10:g.24900786C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2704G>T	ENSP00000384484.2:p.Ala902Ser
ENST00000679454.1:c.2701G>T MANE Select	ENSP00000505261.1:p.Ala901Ser
ENST00000260600.9:c.2701G>T	ENSP00000260600.5:p.Ala901Ser
ENST00000405392.5:c.2704G>T	ENSP00000384484.2:p.Ala902Ser
ENST00000606682.5:c.1642G>T	ENSP00000475652.1:p.Ala548Ser
NM_004036.3:c.2701G>T	NP_004027.2:p.Ala901Ser
XM_005264104.1:c.2704G>T	XP_005264161.1:p.Ala902Ser
XM_005264105.1:c.2701G>T	XP_005264162.1:p.Ala901Ser
XM_006711925.1:c.2770G>T	XP_006711988.1:p.Ala924Ser
XM_011532489.1:c.2827G>T	XP_011530791.1:p.Ala943Ser
XM_011532490.1:c.2824G>T	XP_011530792.1:p.Ala942Ser
XM_011532491.1:c.2761G>T	XP_011530793.1:p.Ala921Ser
XM_011532492.1:c.2827G>T	XP_011530794.1:p.Ala943Ser
XM_011532493.1:c.2689G>T	XP_011530795.1:p.Ala897Ser
XM_011532494.1:c.2629G>T	XP_011530796.1:p.Ala877Ser
XM_011532495.1:c.2161G>T	XP_011530797.1:p.Ala721Ser
XM_011532496.1:c.2104G>T	XP_011530798.1:p.Ala702Ser
NM_001320613.1:c.2704G>T	NP_001307542.1:p.Ala902Ser
NM_004036.4:c.2701G>T	NP_004027.2:p.Ala901Ser
XM_011532492.2:c.2827G>T	XP_011530794.1:p.Ala943Ser
XM_017003186.1:c.2767G>T	XP_016858675.1:p.Ala923Ser
XM_017003187.1:c.2758G>T	XP_016858676.1:p.Ala920Ser
XM_017003188.1:c.2824G>T	XP_016858677.1:p.Ala942Ser
XM_017003189.1:c.2686G>T	XP_016858678.1:p.Ala896Ser
XM_017003190.1:c.2563G>T	XP_016858679.1:p.Ala855Ser
XM_017003191.1:c.2191G>T	XP_016858680.1:p.Ala731Ser
XM_017003192.1:c.1981G>T	XP_016858681.1:p.Ala661Ser
XM_017003193.1:c.1978G>T	XP_016858682.1:p.Ala660Ser
NM_001320613.2:c.2704G>T	NP_001307542.1:p.Ala902Ser
NM_001377128.1:c.2767G>T	NP_001364057.1:p.Ala923Ser
NM_001377129.1:c.2563G>T	NP_001364058.1:p.Ala855Ser
NM_001377130.1:c.2296G>T	NP_001364059.1:p.Ala766Ser
NM_001377131.1:c.1978G>T	NP_001364060.1:p.Ala660Ser
NM_001377132.1:c.2701G>T	NP_001364061.1:p.Ala901Ser
NM_004036.5:c.2701G>T MANE Select	NP_004027.2:p.Ala901Ser