Canonical Allele Identifier: CA13562124
Gene: FAT3 HGNC NCBI
PGAM1P9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.92367190A>T , CM000673.2:g.92367190A>T GRCh38
NC_000011.9:g.92100356A>T , CM000673.1:g.92100356A>T GRCh37
NC_000011.8:g.91740004A>T NCBI36
NG_052813.1:g.147555A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525166.6:c.3292+11786A>T (FAT3) MANE Select ENSP00000432586.2:n.3292+11786A>T
ENST00000409404.6:c.3292+11786A>T (FAT3) ENSP00000387040.2:n.3292+11786A>T
ENST00000503887.1:n.61T>A (PGAM1P9)
ENST00000525166.5:c.2842+11786A>T (FAT3) ENSP00000432586.1:n.2842+11786A>T
ENST00000528921.1:n.219+11786A>T (FAT3)
NM_001008781.2:c.3292+11786A>T (FAT3) NP_001008781.2:n.3292+11786A>T
XM_011542584.1:c.3337+11786A>T (FAT3) XP_011540886.1:n.3337+11786A>T
XM_017017178.2:c.3292+11786A>T (FAT3) XP_016872667.1:n.3292+11786A>T
XM_017017179.2:c.3292+11786A>T (FAT3) XP_016872668.1:n.3292+11786A>T
XM_017017180.1:c.3292+11786A>T (FAT3) XP_016872669.1:n.3292+11786A>T
XM_017017181.2:c.3292+11786A>T (FAT3) XP_016872670.1:n.3292+11786A>T
XM_017017182.2:c.3292+11786A>T (FAT3) XP_016872671.1:n.3292+11786A>T
XM_017017183.2:c.3292+11786A>T (FAT3) XP_016872672.1:n.3292+11786A>T
XM_017017184.2:c.3292+11786A>T (FAT3) XP_016872673.1:n.3292+11786A>T
XM_017017186.1:c.-39+142016A>T (FAT3) XP_016872675.1:n.-39+142016A>T
NM_001367949.1:c.3292+11786A>T (FAT3) NP_001354878.1:n.3292+11786A>T
NM_001367949.2:c.3292+11786A>T (FAT3) MANE Select NP_001354878.1:n.3292+11786A>T
NM_001008781.3:c.3292+11786A>T (FAT3) NP_001008781.2:n.3292+11786A>T
NM_001378141.1:c.3292+11786A>T (FAT3) NP_001365070.1:n.3292+11786A>T