Canonical Allele Identifier: CA346063092

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046214C>A (hg19) ; chr2:g.24823345C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823345C>A , CM000664.2:g.24823345C>A	GRCh38
NC_000002.11:g.25046214C>A , CM000664.1:g.25046214C>A	GRCh37
NC_000002.10:g.24899718C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2750G>T	ENSP00000384484.2:p.Ser917Ile
ENST00000679454.1:c.2747G>T MANE Select	ENSP00000505261.1:p.Ser916Ile
ENST00000260600.9:c.2747G>T	ENSP00000260600.5:p.Ser916Ile
ENST00000405392.5:c.2750G>T	ENSP00000384484.2:p.Ser917Ile
ENST00000485887.1:n.19G>T
ENST00000606682.5:c.1688G>T	ENSP00000475652.1:p.Ser563Ile
NM_004036.3:c.2747G>T	NP_004027.2:p.Ser916Ile
XM_005264104.1:c.2750G>T	XP_005264161.1:p.Ser917Ile
XM_005264105.1:c.2747G>T	XP_005264162.1:p.Ser916Ile
XM_006711925.1:c.2816G>T	XP_006711988.1:p.Ser939Ile
XM_011532489.1:c.2873G>T	XP_011530791.1:p.Ser958Ile
XM_011532490.1:c.2870G>T	XP_011530792.1:p.Ser957Ile
XM_011532491.1:c.2807G>T	XP_011530793.1:p.Ser936Ile
XM_011532492.1:c.2873G>T	XP_011530794.1:p.Ser958Ile
XM_011532493.1:c.2735G>T	XP_011530795.1:p.Ser912Ile
XM_011532494.1:c.2675G>T	XP_011530796.1:p.Ser892Ile
XM_011532495.1:c.2207G>T	XP_011530797.1:p.Ser736Ile
XM_011532496.1:c.2150G>T	XP_011530798.1:p.Ser717Ile
NM_001320613.1:c.2750G>T	NP_001307542.1:p.Ser917Ile
NM_004036.4:c.2747G>T	NP_004027.2:p.Ser916Ile
XM_011532492.2:c.2873G>T	XP_011530794.1:p.Ser958Ile
XM_017003186.1:c.2813G>T	XP_016858675.1:p.Ser938Ile
XM_017003187.1:c.2804G>T	XP_016858676.1:p.Ser935Ile
XM_017003188.1:c.2870G>T	XP_016858677.1:p.Ser957Ile
XM_017003189.1:c.2732G>T	XP_016858678.1:p.Ser911Ile
XM_017003190.1:c.2609G>T	XP_016858679.1:p.Ser870Ile
XM_017003191.1:c.2237G>T	XP_016858680.1:p.Ser746Ile
XM_017003192.1:c.2027G>T	XP_016858681.1:p.Ser676Ile
XM_017003193.1:c.2024G>T	XP_016858682.1:p.Ser675Ile
NM_001320613.2:c.2750G>T	NP_001307542.1:p.Ser917Ile
NM_001377128.1:c.2813G>T	NP_001364057.1:p.Ser938Ile
NM_001377129.1:c.2609G>T	NP_001364058.1:p.Ser870Ile
NM_001377130.1:c.2332-715G>T	NP_001364059.1:n.2332-715G>T
NM_001377131.1:c.2024G>T	NP_001364060.1:p.Ser675Ile
NM_001377132.1:c.2747G>T	NP_001364061.1:p.Ser916Ile
NM_004036.5:c.2747G>T MANE Select	NP_004027.2:p.Ser916Ile