Canonical Allele Identifier: CA4209380
Community Standard Title: NM_001118.5(ADCYAP1R1):c.1294C>T (p.His432Tyr)
Gene: ADCYAP1R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.31106571C>T , CM000669.2:g.31106571C>T GRCh38
NC_000007.13:g.31146185C>T , CM000669.1:g.31146185C>T GRCh37
NC_000007.12:g.31112710C>T NCBI36
NG_029869.1:g.59110C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001118.5:c.1294C>T MANE Select NP_001109.2:p.His432Tyr
ENST00000304166.9:c.1294C>T MANE Select ENSP00000306620.4:p.His432Tyr
NM_001118.4:c.1294C>T NP_001109.2:p.His432Tyr
NM_001199635.1:c.1378C>T NP_001186564.1:p.His460Tyr
NM_001199635.2:c.1378C>T NP_001186564.1:p.His460Tyr
NM_001199636.1:c.1375C>T NP_001186565.1:p.His459Tyr
NM_001199636.2:c.1375C>T NP_001186565.1:p.His459Tyr
NM_001199637.1:c.1231C>T NP_001186566.1:p.His411Tyr
NM_001199637.2:c.1231C>T NP_001186566.1:p.His411Tyr
ENST00000304166.8:c.1294C>T ENSP00000306620.4:p.His432Tyr
ENST00000396211.6:c.1378C>T ENSP00000379514.2:p.His460Tyr
ENST00000396211.7:c.1378C>T ENSP00000379514.2:p.His460Tyr
ENST00000409363.5:c.1231C>T ENSP00000387335.1:p.His411Tyr
ENST00000409489.5:c.1462C>T ENSP00000386395.1:p.His488Tyr
ENST00000614107.4:c.1378C>T ENSP00000483721.1:p.His460Tyr
ENST00000705423.1:c.1375C>T ENSP00000516124.1:p.His459Tyr
ENST00000705424.1:c.1378C>T ENSP00000516125.1:p.His460Tyr
XM_005249618.3:c.1123C>T XP_005249675.1:p.His375Tyr
XM_005249618.5:c.1123C>T XP_005249675.1:p.His375Tyr
XM_006715645.1:c.1378C>T XP_006715708.1:p.His460Tyr
XM_006715645.3:c.1378C>T XP_006715708.1:p.His460Tyr
XM_011515117.1:c.1459C>T XP_011513419.1:p.His487Tyr
XM_011515118.1:c.1438C>T XP_011513420.1:p.His480Tyr
XM_011515119.1:c.1396C>T XP_011513421.1:p.His466Tyr
XM_011515120.1:c.1288C>T XP_011513422.1:p.His430Tyr
XM_017011736.2:c.1357C>T XP_016867225.1:p.His453Tyr
XM_017011737.2:c.1315C>T XP_016867226.1:p.His439Tyr
XM_017011738.2:c.1207C>T XP_016867227.1:p.His403Tyr