Canonical Allele Identifier: CA346063094

Gene: ADCY3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2750G>C	ENSP00000384484.2:p.Ser917Thr
ENST00000679454.1:c.2747G>C MANE Select	ENSP00000505261.1:p.Ser916Thr
ENST00000260600.9:c.2747G>C	ENSP00000260600.5:p.Ser916Thr
ENST00000405392.5:c.2750G>C	ENSP00000384484.2:p.Ser917Thr
ENST00000485887.1:n.19G>C
ENST00000606682.5:c.1688G>C	ENSP00000475652.1:p.Ser563Thr
NM_004036.3:c.2747G>C	NP_004027.2:p.Ser916Thr
XM_005264104.1:c.2750G>C	XP_005264161.1:p.Ser917Thr
XM_005264105.1:c.2747G>C	XP_005264162.1:p.Ser916Thr
XM_006711925.1:c.2816G>C	XP_006711988.1:p.Ser939Thr
XM_011532489.1:c.2873G>C	XP_011530791.1:p.Ser958Thr
XM_011532490.1:c.2870G>C	XP_011530792.1:p.Ser957Thr
XM_011532491.1:c.2807G>C	XP_011530793.1:p.Ser936Thr
XM_011532492.1:c.2873G>C	XP_011530794.1:p.Ser958Thr
XM_011532493.1:c.2735G>C	XP_011530795.1:p.Ser912Thr
XM_011532494.1:c.2675G>C	XP_011530796.1:p.Ser892Thr
XM_011532495.1:c.2207G>C	XP_011530797.1:p.Ser736Thr
XM_011532496.1:c.2150G>C	XP_011530798.1:p.Ser717Thr
NM_001320613.1:c.2750G>C	NP_001307542.1:p.Ser917Thr
NM_004036.4:c.2747G>C	NP_004027.2:p.Ser916Thr
XM_011532492.2:c.2873G>C	XP_011530794.1:p.Ser958Thr
XM_017003186.1:c.2813G>C	XP_016858675.1:p.Ser938Thr
XM_017003187.1:c.2804G>C	XP_016858676.1:p.Ser935Thr
XM_017003188.1:c.2870G>C	XP_016858677.1:p.Ser957Thr
XM_017003189.1:c.2732G>C	XP_016858678.1:p.Ser911Thr
XM_017003190.1:c.2609G>C	XP_016858679.1:p.Ser870Thr
XM_017003191.1:c.2237G>C	XP_016858680.1:p.Ser746Thr
XM_017003192.1:c.2027G>C	XP_016858681.1:p.Ser676Thr
XM_017003193.1:c.2024G>C	XP_016858682.1:p.Ser675Thr
NM_001320613.2:c.2750G>C	NP_001307542.1:p.Ser917Thr
NM_001377128.1:c.2813G>C	NP_001364057.1:p.Ser938Thr
NM_001377129.1:c.2609G>C	NP_001364058.1:p.Ser870Thr
NM_001377130.1:c.2332-715G>C	NP_001364059.1:n.2332-715G>C
NM_001377131.1:c.2024G>C	NP_001364060.1:p.Ser675Thr
NM_001377132.1:c.2747G>C	NP_001364061.1:p.Ser916Thr
NM_004036.5:c.2747G>C MANE Select	NP_004027.2:p.Ser916Thr