Canonical Allele Identifier: CA346062911

Gene: ADCY3

Linked Data

• MyVariant Identifiers: chr2:g.25046173G>T (hg19) ; chr2:g.24823304G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823304G>T , CM000664.2:g.24823304G>T	GRCh38
NC_000002.11:g.25046173G>T , CM000664.1:g.25046173G>T	GRCh37
NC_000002.10:g.24899677G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2791C>A	ENSP00000384484.2:p.Pro931Thr
ENST00000679454.1:c.2788C>A MANE Select	ENSP00000505261.1:p.Pro930Thr
ENST00000260600.9:c.2788C>A	ENSP00000260600.5:p.Pro930Thr
ENST00000405392.5:c.2791C>A	ENSP00000384484.2:p.Pro931Thr
ENST00000485887.1:n.60C>A
ENST00000606682.5:c.1729C>A	ENSP00000475652.1:p.Pro577Thr
NM_004036.3:c.2788C>A	NP_004027.2:p.Pro930Thr
XM_005264104.1:c.2791C>A	XP_005264161.1:p.Pro931Thr
XM_005264105.1:c.2788C>A	XP_005264162.1:p.Pro930Thr
XM_006711925.1:c.2857C>A	XP_006711988.1:p.Pro953Thr
XM_011532489.1:c.2914C>A	XP_011530791.1:p.Pro972Thr
XM_011532490.1:c.2911C>A	XP_011530792.1:p.Pro971Thr
XM_011532491.1:c.2848C>A	XP_011530793.1:p.Pro950Thr
XM_011532492.1:c.2914C>A	XP_011530794.1:p.Pro972Thr
XM_011532493.1:c.2776C>A	XP_011530795.1:p.Pro926Thr
XM_011532494.1:c.2716C>A	XP_011530796.1:p.Pro906Thr
XM_011532495.1:c.2248C>A	XP_011530797.1:p.Pro750Thr
XM_011532496.1:c.2191C>A	XP_011530798.1:p.Pro731Thr
NM_001320613.1:c.2791C>A	NP_001307542.1:p.Pro931Thr
NM_004036.4:c.2788C>A	NP_004027.2:p.Pro930Thr
XM_011532492.2:c.2914C>A	XP_011530794.1:p.Pro972Thr
XM_017003186.1:c.2854C>A	XP_016858675.1:p.Pro952Thr
XM_017003187.1:c.2845C>A	XP_016858676.1:p.Pro949Thr
XM_017003188.1:c.2911C>A	XP_016858677.1:p.Pro971Thr
XM_017003189.1:c.2773C>A	XP_016858678.1:p.Pro925Thr
XM_017003190.1:c.2650C>A	XP_016858679.1:p.Pro884Thr
XM_017003191.1:c.2278C>A	XP_016858680.1:p.Pro760Thr
XM_017003192.1:c.2068C>A	XP_016858681.1:p.Pro690Thr
XM_017003193.1:c.2065C>A	XP_016858682.1:p.Pro689Thr
NM_001320613.2:c.2791C>A	NP_001307542.1:p.Pro931Thr
NM_001377128.1:c.2854C>A	NP_001364057.1:p.Pro952Thr
NM_001377129.1:c.2650C>A	NP_001364058.1:p.Pro884Thr
NM_001377130.1:c.2332-674C>A	NP_001364059.1:n.2332-674C>A
NM_001377131.1:c.2065C>A	NP_001364060.1:p.Pro689Thr
NM_001377132.1:c.2788C>A	NP_001364061.1:p.Pro930Thr
NM_004036.5:c.2788C>A MANE Select	NP_004027.2:p.Pro930Thr