Canonical Allele Identifier: CA346062902
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823303G>A , CM000664.2:g.24823303G>A GRCh38
NC_000002.11:g.25046172G>A , CM000664.1:g.25046172G>A GRCh37
NC_000002.10:g.24899676G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2792C>T ENSP00000384484.2:p.Pro931Leu
ENST00000679454.1:c.2789C>T MANE Select ENSP00000505261.1:p.Pro930Leu
ENST00000260600.9:c.2789C>T ENSP00000260600.5:p.Pro930Leu
ENST00000405392.5:c.2792C>T ENSP00000384484.2:p.Pro931Leu
ENST00000485887.1:n.61C>T
ENST00000606682.5:c.1730C>T ENSP00000475652.1:p.Pro577Leu
NM_004036.3:c.2789C>T NP_004027.2:p.Pro930Leu
XM_005264104.1:c.2792C>T XP_005264161.1:p.Pro931Leu
XM_005264105.1:c.2789C>T XP_005264162.1:p.Pro930Leu
XM_006711925.1:c.2858C>T XP_006711988.1:p.Pro953Leu
XM_011532489.1:c.2915C>T XP_011530791.1:p.Pro972Leu
XM_011532490.1:c.2912C>T XP_011530792.1:p.Pro971Leu
XM_011532491.1:c.2849C>T XP_011530793.1:p.Pro950Leu
XM_011532492.1:c.2915C>T XP_011530794.1:p.Pro972Leu
XM_011532493.1:c.2777C>T XP_011530795.1:p.Pro926Leu
XM_011532494.1:c.2717C>T XP_011530796.1:p.Pro906Leu
XM_011532495.1:c.2249C>T XP_011530797.1:p.Pro750Leu
XM_011532496.1:c.2192C>T XP_011530798.1:p.Pro731Leu
NM_001320613.1:c.2792C>T NP_001307542.1:p.Pro931Leu
NM_004036.4:c.2789C>T NP_004027.2:p.Pro930Leu
XM_011532492.2:c.2915C>T XP_011530794.1:p.Pro972Leu
XM_017003186.1:c.2855C>T XP_016858675.1:p.Pro952Leu
XM_017003187.1:c.2846C>T XP_016858676.1:p.Pro949Leu
XM_017003188.1:c.2912C>T XP_016858677.1:p.Pro971Leu
XM_017003189.1:c.2774C>T XP_016858678.1:p.Pro925Leu
XM_017003190.1:c.2651C>T XP_016858679.1:p.Pro884Leu
XM_017003191.1:c.2279C>T XP_016858680.1:p.Pro760Leu
XM_017003192.1:c.2069C>T XP_016858681.1:p.Pro690Leu
XM_017003193.1:c.2066C>T XP_016858682.1:p.Pro689Leu
NM_001320613.2:c.2792C>T NP_001307542.1:p.Pro931Leu
NM_001377128.1:c.2855C>T NP_001364057.1:p.Pro952Leu
NM_001377129.1:c.2651C>T NP_001364058.1:p.Pro884Leu
NM_001377130.1:c.2332-673C>T NP_001364059.1:n.2332-673C>T
NM_001377131.1:c.2066C>T NP_001364060.1:p.Pro689Leu
NM_001377132.1:c.2789C>T NP_001364061.1:p.Pro930Leu
NM_004036.5:c.2789C>T MANE Select NP_004027.2:p.Pro930Leu