Canonical Allele Identifier: CA2662343386

Gene: PMS1

Linked Data

• gnomAD v4: 2-189784385-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189784385T>A , CM000664.2:g.189784385T>A	GRCh38
NC_000002.11:g.190649111T>A , CM000664.1:g.190649111T>A	GRCh37
NC_000002.10:g.190357356T>A	NCBI36
NG_008648.1:g.5301T>A , LRG_221:g.5301T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639501.1:c.-229T>A	ENSP00000491236.1:n.-229T>A
ENST00000418224.7:c.-229T>A	ENSP00000404492.4:n.-229T>A
ENST00000432292.7:c.-471T>A	ENSP00000398378.3:n.-471T>A
ENST00000441310.6:c.-229T>A	ENSP00000406490.2:n.-229T>A
ENST00000618056.4:c.-229T>A	ENSP00000480632.1:n.-229T>A
ENST00000624204.3:c.-654T>A	ENSP00000485312.1:n.-654T>A
NM_000534.4:c.-229T>A , LRG_221t1:c.-229T>A	NP_000525.1:n.-229T>A
NM_001128143.1:c.-229T>A	NP_001121615.1:n.-229T>A
NM_001128144.1:c.-229T>A	NP_001121616.1:n.-229T>A
NM_001289408.1:c.-654T>A	NP_001276337.1:n.-654T>A
NM_001289409.1:c.-471T>A	NP_001276338.1:n.-471T>A
NR_110332.1:n.301T>A
NM_001321044.1:c.-229T>A	NP_001307973.1:n.-229T>A
NM_001321045.1:c.-355T>A	NP_001307974.1:n.-355T>A
NM_001321046.1:c.-229T>A	NP_001307975.1:n.-229T>A
NM_001321047.1:c.-406T>A	NP_001307976.1:n.-406T>A
NM_001321048.1:c.-326T>A	NP_001307977.1:n.-326T>A
NM_001321049.1:c.-229T>A	NP_001307978.1:n.-229T>A
NM_001321051.1:c.-229T>A	NP_001307980.1:n.-229T>A
XM_024452965.1:c.-200T>A	XP_024308733.1:n.-200T>A