Canonical Allele Identifier: CA2662343402
Gene: PMS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189784414G>T , CM000664.2:g.189784414G>T GRCh38
NC_000002.11:g.190649140G>T , CM000664.1:g.190649140G>T GRCh37
NC_000002.10:g.190357385G>T NCBI36
NG_008648.1:g.5330G>T , LRG_221:g.5330G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000639501.1:c.-200G>T ENSP00000491236.1:n.-200G>T
ENST00000418224.7:c.-200G>T ENSP00000404492.4:n.-200G>T
ENST00000432292.7:c.-442G>T ENSP00000398378.3:n.-442G>T
ENST00000441310.6:c.-200G>T ENSP00000406490.2:n.-200G>T
ENST00000618056.4:c.-200G>T ENSP00000480632.1:n.-200G>T
ENST00000624204.3:c.-625G>T ENSP00000485312.1:n.-625G>T
NM_000534.4:c.-200G>T , LRG_221t1:c.-200G>T NP_000525.1:n.-200G>T
NM_001128143.1:c.-200G>T NP_001121615.1:n.-200G>T
NM_001128144.1:c.-200G>T NP_001121616.1:n.-200G>T
NM_001289408.1:c.-625G>T NP_001276337.1:n.-625G>T
NM_001289409.1:c.-442G>T NP_001276338.1:n.-442G>T
NR_110332.1:n.330G>T
NM_001321044.1:c.-200G>T NP_001307973.1:n.-200G>T
NM_001321045.1:c.-326G>T NP_001307974.1:n.-326G>T
NM_001321046.1:c.-200G>T NP_001307975.1:n.-200G>T
NM_001321047.1:c.-377G>T NP_001307976.1:n.-377G>T
NM_001321048.1:c.-297G>T NP_001307977.1:n.-297G>T
NM_001321049.1:c.-200G>T NP_001307978.1:n.-200G>T
NM_001321051.1:c.-200G>T NP_001307980.1:n.-200G>T
XM_024452965.1:c.-171G>T XP_024308733.1:n.-171G>T