Canonical Allele Identifier: CA1315746075

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189784357C= , CM000664.2:g.189784357C= GRCh38
NC_000002.11:g.190649083C= , CM000664.1:g.190649083C= GRCh37
NC_000002.10:g.190357328C= NCBI36
NG_008648.1:g.5273C= , LRG_221:g.5273C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000639501.1:c.-257C= (PMS1) ENSP00000491236.1:n.-257C=
ENST00000392349.8:c.-206G= (ORMDL1) ENSP00000376160.4:n.-206G=
ENST00000392350.7:c.-96G= (ORMDL1) ENSP00000376161.3:n.-96G=
ENST00000418224.7:c.-257C= (PMS1) ENSP00000404492.4:n.-257C=
ENST00000432292.7:c.-499C= (PMS1) ENSP00000398378.3:n.-499C=
ENST00000618056.4:c.-257C= (PMS1) ENSP00000480632.1:n.-257C=
ENST00000624204.3:c.-682C= (PMS1) ENSP00000485312.1:n.-682C=
NM_000534.4:c.-257C= , LRG_221t1:c.-257C= (PMS1) NP_000525.1:n.-257C=
NM_001128143.1:c.-257C= (PMS1) NP_001121615.1:n.-257C=
NM_001128144.1:c.-257C= (PMS1) NP_001121616.1:n.-257C=
NM_001128150.1:c.-96G= (ORMDL1) NP_001121622.1:n.-96G=
NM_001289408.1:c.-682C= (PMS1) NP_001276337.1:n.-682C=
NM_001289409.1:c.-499C= (PMS1) NP_001276338.1:n.-499C=
NM_016467.4:c.-206G= (ORMDL1) NP_057551.1:n.-206G=
NR_110332.1:n.273C= (PMS1)
NM_001321044.1:c.-257C= (PMS1) NP_001307973.1:n.-257C=
NM_001321045.1:c.-383C= (PMS1) NP_001307974.1:n.-383C=
NM_001321046.1:c.-257C= (PMS1) NP_001307975.1:n.-257C=
NM_001321047.1:c.-434C= (PMS1) NP_001307976.1:n.-434C=
NM_001321048.1:c.-354C= (PMS1) NP_001307977.1:n.-354C=
NM_001321049.1:c.-257C= (PMS1) NP_001307978.1:n.-257C=
NM_001321051.1:c.-257C= (PMS1) NP_001307980.1:n.-257C=
XM_011512199.3:c.-96G= (ORMDL1) XP_011510501.1:n.-96G=
XM_024452965.1:c.-228C= (PMS1) XP_024308733.1:n.-228C=