Canonical Allele Identifier: CA2662343394
Gene: PMS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189784408A>G , CM000664.2:g.189784408A>G GRCh38
NC_000002.11:g.190649134A>G , CM000664.1:g.190649134A>G GRCh37
NC_000002.10:g.190357379A>G NCBI36
NG_008648.1:g.5324A>G , LRG_221:g.5324A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000639501.1:c.-206A>G ENSP00000491236.1:n.-206A>G
ENST00000418224.7:c.-206A>G ENSP00000404492.4:n.-206A>G
ENST00000432292.7:c.-448A>G ENSP00000398378.3:n.-448A>G
ENST00000441310.6:c.-206A>G ENSP00000406490.2:n.-206A>G
ENST00000618056.4:c.-206A>G ENSP00000480632.1:n.-206A>G
ENST00000624204.3:c.-631A>G ENSP00000485312.1:n.-631A>G
NM_000534.4:c.-206A>G , LRG_221t1:c.-206A>G NP_000525.1:n.-206A>G
NM_001128143.1:c.-206A>G NP_001121615.1:n.-206A>G
NM_001128144.1:c.-206A>G NP_001121616.1:n.-206A>G
NM_001289408.1:c.-631A>G NP_001276337.1:n.-631A>G
NM_001289409.1:c.-448A>G NP_001276338.1:n.-448A>G
NR_110332.1:n.324A>G
NM_001321044.1:c.-206A>G NP_001307973.1:n.-206A>G
NM_001321045.1:c.-332A>G NP_001307974.1:n.-332A>G
NM_001321046.1:c.-206A>G NP_001307975.1:n.-206A>G
NM_001321047.1:c.-383A>G NP_001307976.1:n.-383A>G
NM_001321048.1:c.-303A>G NP_001307977.1:n.-303A>G
NM_001321049.1:c.-206A>G NP_001307978.1:n.-206A>G
NM_001321051.1:c.-206A>G NP_001307980.1:n.-206A>G
XM_024452965.1:c.-177A>G XP_024308733.1:n.-177A>G