Canonical Allele Identifier: CA1315746210
Gene: PMS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189784522C= , CM000664.2:g.189784522C= GRCh38
NC_000002.11:g.190649248C= , CM000664.1:g.190649248C= GRCh37
NC_000002.10:g.190357493C= NCBI36
NG_008648.1:g.5438C= , LRG_221:g.5438C=

Transcript Alleles

HGVS Amino-acid change
ENST00000441310.7:c.-92C= MANE Select ENSP00000406490.3:n.-92C=
ENST00000639501.1:c.-92C= ENSP00000491236.1:n.-92C=
ENST00000342075.8:c.-92C= ENSP00000343888.4:n.-92C=
ENST00000374826.8:c.-92C= ENSP00000363959.4:n.-92C=
ENST00000409823.7:c.-92C= ENSP00000387125.3:n.-92C=
ENST00000409985.5:c.-92C= ENSP00000386623.1:n.-92C=
ENST00000418224.7:c.-92C= ENSP00000404492.4:n.-92C=
ENST00000432292.7:c.-334C= ENSP00000398378.3:n.-334C=
ENST00000441310.6:c.-92C= ENSP00000406490.2:n.-92C=
ENST00000446877.5:c.-395C= ENSP00000413837.1:n.-395C=
ENST00000450931.5:c.-189C= ENSP00000406225.1:n.-189C=
ENST00000618056.4:c.-92C= ENSP00000480632.1:n.-92C=
ENST00000624204.3:c.-517C= ENSP00000485312.1:n.-517C=
NM_000534.4:c.-92C= , LRG_221t1:c.-92C= NP_000525.1:n.-92C=
NM_001128143.1:c.-92C= NP_001121615.1:n.-92C=
NM_001128144.1:c.-92C= NP_001121616.1:n.-92C=
NM_001289408.1:c.-517C= NP_001276337.1:n.-517C=
NM_001289409.1:c.-334C= NP_001276338.1:n.-334C=
NR_110332.1:n.438C=
XM_005246647.2:c.-218C= XP_005246704.1:n.-218C=
XM_005246649.2:c.-92C= XP_005246706.1:n.-92C=
XM_011511354.1:c.-189C= XP_011509656.1:n.-189C=
XM_011511355.1:c.-92C= XP_011509657.1:n.-92C=
XM_011511357.1:c.-92C= XP_011509659.1:n.-92C=
XR_922951.1:n.73C=
NM_001321044.1:c.-92C= NP_001307973.1:n.-92C=
NM_001321045.1:c.-218C= NP_001307974.1:n.-218C=
NM_001321046.1:c.-92C= NP_001307975.1:n.-92C=
NM_001321047.1:c.-269C= NP_001307976.1:n.-269C=
NM_001321048.1:c.-189C= NP_001307977.1:n.-189C=
NM_001321049.1:c.-92C= NP_001307978.1:n.-92C=
NM_001321051.1:c.-92C= NP_001307980.1:n.-92C=
XM_011511356.3:c.-1415C= XP_011509658.1:n.-1415C=
XM_017004344.1:c.-218C= XP_016859833.1:n.-218C=
XM_017004345.1:c.-113C= XP_016859834.1:n.-113C=
XM_017004346.2:c.-63C= XP_016859835.1:n.-63C=
XM_017004347.1:c.-92C= XP_016859836.1:n.-92C=
XM_017004350.1:c.-92C= XP_016859839.1:n.-92C=
XM_024452964.1:c.-113C= XP_024308732.1:n.-113C=
XM_024452965.1:c.-63C= XP_024308733.1:n.-63C=
XM_024452966.1:c.-113C= XP_024308734.1:n.-113C=
XM_024452967.1:c.-63C= XP_024308735.1:n.-63C=
XM_024452968.1:c.-488C= XP_024308736.1:n.-488C=
XM_024452969.1:c.-517C= XP_024308737.1:n.-517C=
XR_001738779.1:n.38C=
XR_002959307.1:n.22C=
XR_922951.2:n.67C=
NM_000534.5:c.-92C= MANE Select NP_000525.1:n.-92C=
NM_001128143.2:c.-92C= NP_001121615.1:n.-92C=
NM_001128144.2:c.-92C= NP_001121616.1:n.-92C=
NM_001321044.2:c.-92C= NP_001307973.1:n.-92C=
NM_001321045.2:c.-218C= NP_001307974.1:n.-218C=
NM_001321046.2:c.-92C= NP_001307975.1:n.-92C=
NM_001321047.2:c.-269C= NP_001307976.1:n.-269C=
NM_001321048.2:c.-189C= NP_001307977.1:n.-189C=
NM_001321049.2:c.-92C= NP_001307978.1:n.-92C=
NR_110332.2:n.73C=
NM_001289408.2:c.-517C= NP_001276337.1:n.-517C=
NM_001289409.2:c.-334C= NP_001276338.1:n.-334C=
NM_001321051.2:c.-92C= NP_001307980.1:n.-92C=